CN101305023B - Polymer having sulfonic acid group or sulfonic acid ester group and amide group, and toner for developing electrostatic latent image having the polymer - Google Patents

Polymer having sulfonic acid group or sulfonic acid ester group and amide group, and toner for developing electrostatic latent image having the polymer Download PDF

Info

Publication number
CN101305023B
CN101305023B CN2006800415696A CN200680041569A CN101305023B CN 101305023 B CN101305023 B CN 101305023B CN 2006800415696 A CN2006800415696 A CN 2006800415696A CN 200680041569 A CN200680041569 A CN 200680041569A CN 101305023 B CN101305023 B CN 101305023B
Authority
CN
China
Prior art keywords
replacement
polymkeric substance
chemical formula
expression
base
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
CN2006800415696A
Other languages
Chinese (zh)
Other versions
CN101305023A (en
Inventor
福井树
富永明子
见目敬
南昌人
矢野哲哉
池田武志
谷笃
藤本则和
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Canon Inc
Original Assignee
Canon Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Canon Inc filed Critical Canon Inc
Publication of CN101305023A publication Critical patent/CN101305023A/en
Application granted granted Critical
Publication of CN101305023B publication Critical patent/CN101305023B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00—Developers
    • G03G9/08—Developers with toner particles
    • G03G9/087—Binders for toner particles
    • G03G9/08702—Binders for toner particles comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • G03G9/08724—Polyvinylesters
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F12/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
    • C08F12/02—Monomers containing only one unsaturated aliphatic radical
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/01—Sulfonic acids
    • C07C309/28—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C309/45—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton
    • C07C309/51—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton at least one of the nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/63—Esters of sulfonic acids
    • C07C309/72—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C309/76—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/78—Halides of sulfonic acids
    • C07C309/86—Halides of sulfonic acids having halosulfonyl groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C309/88—Halides of sulfonic acids having halosulfonyl groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F12/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
    • C08F12/02—Monomers containing only one unsaturated aliphatic radical
    • C08F12/04—Monomers containing only one unsaturated aliphatic radical containing one ring
    • C08F12/14—Monomers containing only one unsaturated aliphatic radical containing one ring substituted by hetero atoms or groups containing heteroatoms
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F12/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
    • C08F12/02—Monomers containing only one unsaturated aliphatic radical
    • C08F12/04—Monomers containing only one unsaturated aliphatic radical containing one ring
    • C08F12/14—Monomers containing only one unsaturated aliphatic radical containing one ring substituted by hetero atoms or groups containing heteroatoms
    • C08F12/26—Nitrogen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F12/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
    • C08F12/02—Monomers containing only one unsaturated aliphatic radical
    • C08F12/04—Monomers containing only one unsaturated aliphatic radical containing one ring
    • C08F12/14—Monomers containing only one unsaturated aliphatic radical containing one ring substituted by hetero atoms or groups containing heteroatoms
    • C08F12/30—Sulfur
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F12/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
    • C08F12/02—Monomers containing only one unsaturated aliphatic radical
    • C08F12/32—Monomers containing only one unsaturated aliphatic radical containing two or more rings
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F212/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
    • C08F212/02—Monomers containing only one unsaturated aliphatic radical
    • C08F212/04—Monomers containing only one unsaturated aliphatic radical containing one ring
    • C08F212/14—Monomers containing only one unsaturated aliphatic radical containing one ring substituted by heteroatoms or groups containing heteroatoms
    • C08F212/16—Halogens
    • C08F212/18—Chlorine
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F212/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
    • C08F212/02—Monomers containing only one unsaturated aliphatic radical
    • C08F212/04—Monomers containing only one unsaturated aliphatic radical containing one ring
    • C08F212/14—Monomers containing only one unsaturated aliphatic radical containing one ring substituted by heteroatoms or groups containing heteroatoms
    • C08F212/30—Sulfur
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F212/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
    • C08F212/02—Monomers containing only one unsaturated aliphatic radical
    • C08F212/32—Monomers containing only one unsaturated aliphatic radical containing two or more rings
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00—Chemical modification by after-treatment
    • C08F8/02—Alkylation
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00—Chemical modification by after-treatment
    • C08F8/34—Introducing sulfur atoms or sulfur-containing groups
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00—Developers
    • G03G9/08—Developers with toner particles
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00—Developers
    • G03G9/08—Developers with toner particles
    • G03G9/087—Binders for toner particles
    • G03G9/08702—Binders for toner particles comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • G03G9/08726—Polymers of unsaturated acids or derivatives thereof
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00—Developers
    • G03G9/08—Developers with toner particles
    • G03G9/087—Binders for toner particles
    • G03G9/08702—Binders for toner particles comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • G03G9/08726—Polymers of unsaturated acids or derivatives thereof
    • G03G9/08728—Polymers of esters
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00—Developers
    • G03G9/08—Developers with toner particles
    • G03G9/087—Binders for toner particles
    • G03G9/08784—Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775
    • G03G9/08791—Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775 characterised by the presence of specified groups or side chains
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F212/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
    • C08F212/02—Monomers containing only one unsaturated aliphatic radical
    • C08F212/04—Monomers containing only one unsaturated aliphatic radical containing one ring
    • C08F212/06—Hydrocarbons
    • C08F212/08—Styrene

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physics & Mathematics (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • General Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

There is provided a polymer including a unit represented by Chemical Formula (1): wherein R represents -A1-SO2R1; R1w and R1X are each independently a halogen atom or a hydrogen atom; R1y is a CH3 group, a halogen atom or a hydrogen atom; A01 is a substituted or unsubstituted aromatic ring structure or a substituted or unsubstituted heterocyclic structure; A1 is a substituted or unsubstituted aliphatic hydrocarbon structure, a substituted or unsubstituted aromatic ring structure or a substituted or unsubstituted heterocyclic structure; R1 is OH, a halogen atom, ONa, OK or OR1a; R1a is a substituted or unsubstituted aliphatic hydrocarbon structure, a substituted or unsubstituted aromatic ring structure or a substituted or unsubstituted heterocyclic structure.

Description

Have the polymkeric substance of sulfonic group or sulfonate group and amide group, and the toning agent that is used for developing electrostatic latent image with this polymkeric substance
Technical field
The present invention relates to have the new polymers of sulfonic group or sulfonate group and amide group.In addition, the present invention relates to be used to produce the novel cpd of above-mentioned new polymers.And, the present invention relates to comprise the toning agent that is used for developing electrostatic latent image of above-mentioned new polymers.
Background technology
Expectation is used for various uses with possess hydrophilic property group such as sulfonic polymkeric substance.Usually, the synthetic method that comprises this sulfonic polymkeric substance is limited to and uses the special ethylene base monomer methods that comprises the sulfonic acid functional group.
This monomeric particular instance comprises sulfonated phenylethylene or AMPS (2-acrylamido-2-methyl propane sulfonic acid).
For example, the 2-acrylamido-2-methyl propane sulfonic acid salt of the open example as sulfonated phenylethylene of Japanese Patent Application Laid-Open 2002-351147 and other can with the multipolymer of the vinyl monomer of its copolymerization.
Summary of the invention
Yet not talkative only sulfonated phenylethylene just fully satisfies above-mentioned various uses, and requires further to improve and the development of new polymkeric substance.Consider above background technology, an object of the present invention is to provide new polymers and production method thereof with sulfonic group or sulfonate group and amide group.Another object of the present invention provides the novel cpd that is used to produce above-mentioned polymkeric substance.A further object of the present invention provides the toning agent that is used for developing electrostatic latent image that uses above-mentioned polymkeric substance.
Therefore, the inventor furthers investigate at the development of new polymkeric substance, has introduced polar group or hydrophilic radical and think that it is useful to improving various functionality in this polymkeric substance, and the result finishes following invention.
Polymkeric substance of the present invention is for being characterised in that the unitary polymkeric substance that comprises by chemical formula (1) expression:
(wherein R represents-A 1-SO 2R 1R 1wAnd R 1xBe halogen atom or hydrogen atom independently of one another.R 1yBe CH 3Base, halogen atom or hydrogen atom.
A 01For replacing or the aromatic ring structure of non-replacement or the heterocycle structure of replacement or non-replacement.
A 1For replacing or the aromatic ring structure of aliphatic hydrocrbon structure, replacement or the non-replacement of non-replacement or the heterocycle structure of replacement or non-replacement.
R 1Be OH, halogen atom, ONa, OK or OR 1aR 1aFor replacing or the aromatic ring structure of aliphatic hydrocrbon structure, replacement or the non-replacement of non-replacement or the heterocycle structure of replacement or non-replacement).
As the monomeric useful compound that is used for production polymkeric substance of the present invention, be characterised in that the structure that has by chemical formula (201) expression:
Figure S2006800415696D00031
(wherein R represents-A 201-SO 2R 201R 201wAnd R 201XBe halogen atom or hydrogen atom independently of one another.R 201yBe CH 3Base, halogen atom or hydrogen atom.
A 0201For replacing or the aromatic ring structure of non-replacement or the heterocycle structure of replacement or non-replacement.A 201For replacing or the aromatic ring structure of aliphatic hydrocrbon structure, replacement or the non-replacement of non-replacement or the heterocycle structure of replacement or non-replacement.
R 201Be OH, halogen atom, ONa, OK or OR 201aR 201aFor replacing or the aromatic ring structure of aliphatic hydrocrbon structure, replacement or the non-replacement of non-replacement or the heterocycle structure of replacement or non-replacement).
Another embodiment of the production method of polymkeric substance of the present invention comprises following production method.
That is, it is to be characterised in that following production method: the unitary polymkeric substance and at least a amine compound of being represented by chemical formula (302) that will comprise by chemical formula (301) expression carry out condensation reaction to obtain comprising the unitary polymkeric substance by chemical formula (1) expression.
Figure S2006800415696D00041
(R wherein 301wAnd R 301xBe halogen atom or hydrogen atom independently of one another.R 301yBe CH 3Base, halogen atom or hydrogen atom.R 301Be H atom, Na atom or K atom).
H 2N-A 302-SO 2R 302 (302)
(R wherein 302Be OH, halogen atom, ONa, OK or OR 302aA 302And R 302aIndependently of one another for replacing or the aromatic ring structure of aliphatic hydrocrbon structure, replacement or the non-replacement of non-replacement or the heterocycle structure of replacement or non-replacement).
Figure S2006800415696D00042
(wherein R represents-A 1-SO 2R 1R 1wAnd R 1xBe halogen atom or hydrogen atom independently of one another.R 1yBe CH 3Base, halogen atom or hydrogen atom.
A 01For replacing or the aromatic ring structure of non-replacement or the heterocycle structure of replacement or non-replacement.
A 1For replacing or the aromatic ring structure of aliphatic hydrocrbon structure, replacement or the non-replacement of non-replacement or the heterocycle structure of replacement or non-replacement.
R 1Be OH, halogen atom, ONa, OK or OR 1a
R 1aFor replacing or the aromatic ring structure of aliphatic hydrocrbon structure, replacement or the non-replacement of non-replacement or the heterocycle structure of replacement or non-replacement).
Another embodiment of method for producing polymer of the present invention comprises and is characterised in that following production method: the unitary polymkeric substance that uses esterifying agent to make to comprise by chemical formula (303) expression carries out esterification to obtain comprising the unitary polymkeric substance by chemical formula (304) expression.
Figure S2006800415696D00051
(wherein R represents-A 303-SO 2R 303R 303wAnd R 303XBe halogen atom or hydrogen atom independently of one another.R 303yBe CH 3Base, halogen atom or hydrogen atom.
A 0303For replacing or the aromatic ring structure of non-replacement or the heterocycle structure of replacement or non-replacement.
A 303For replacing or the aromatic ring structure of aliphatic hydrocrbon structure, replacement or the non-replacement of non-replacement or the heterocycle structure of replacement or non-replacement.R 303Be OH, halogen atom, ONa or OK).
Figure S2006800415696D00061
(wherein R represents-A 304-SO 3R 304R 304wAnd R 304XBe halogen atom or hydrogen atom independently of one another.R 304yBe CH 3Base, halogen atom or hydrogen atom.
A 0304For replacing or the aromatic ring structure of non-replacement or the heterocycle structure of replacement or non-replacement.
A 304For replacing or the aromatic ring structure of aliphatic hydrocrbon structure, replacement or the non-replacement of non-replacement or the heterocycle structure of replacement or non-replacement.
R 304For replacing or the aromatic ring structure of aliphatic hydrocrbon structure, replacement or the non-replacement of non-replacement or the heterocycle structure of replacement or non-replacement).
Charge control agent of the present invention is the charge control agent of control fine particle electriferous state, and wherein this charge control agent comprises a kind of above-mentioned polymkeric substance at least.
The toning agent that is used for developing electrostatic latent image according to the present invention is to be characterised in that the following toning agent that is used for developing electrostatic latent image: this toning agent that is used for developing electrostatic latent image comprises the polymkeric substance of resin glue, tinting material and the invention described above at least.At this, above-mentioned polymkeric substance is preferably as the charge control agent of this toning agent.
According to the present invention, provide the novel cpd of new polymers and this polymkeric substance of production.In addition, can provide the toning agent that is used for developing electrostatic latent image that uses above polymkeric substance.
Description of drawings
Fig. 1 illustrates among the embodiment R-0 1The diagram of H-NMR measuring result;
Fig. 2 illustrates among the embodiment S-0 1The diagram of H-NMR measuring result;
Fig. 3 illustrates among the embodiment T-1 1The diagram of H-NMR measuring result;
Fig. 4 illustrates among the embodiment T-2 1The diagram of H-NMR measuring result; With
Fig. 5 is the synoptic diagram that the emptying zone coulometry equipment (blow off zone coulometry apparatus) that is used to measure the toning agent carried charge is shown.
In Fig. 5, Reference numeral 41 expressions are used to measure the device of carried charge, the container that 42 expressions are used to measure, 43 expression sieves, 44 expression lids, 45 expression vacuumometers, 46 expressions are used for the valve of control air air flow, 47 expression pump orifices, 48 expression electrical condensers, 49 expression potentiometers.
Embodiment
(polymkeric substance of the present invention and compound)
Polymer features of the present invention is to comprise one or more unit by above-mentioned chemical formula (1) expression structure.
Simultaneously, when having a plurality of unit in this polymkeric substance, each unit is represented by various definition independent of each other among the present invention.For example, can exist a plurality of same units maybe can have the different units of representing by formula (1) by formula (1) expression.This point is also applicable to the unit of being represented by other formula.That is, the present invention not only comprises the situation that above polymkeric substance is made up of the unit of same type, also comprises the situation that above polymkeric substance is made up of dissimilar unit.
As the unit by chemical formula (1) expression of polymkeric substance of the present invention, the unit of preferred chemical formula (2) to (11).
Figure S2006800415696D00081
(wherein R represents-A 2-SO 2R 2R 2wAnd R 2XBe halogen atom or hydrogen atom independently of one another.R 2yBe CH 3Base, halogen atom or hydrogen atom.
A 02For replacing or the aromatic ring structure of non-replacement or the heterocycle structure of replacement or non-replacement.
A 2For replacing or the aromatic ring structure of aliphatic hydrocrbon structure, replacement or the non-replacement of non-replacement or the heterocycle structure of replacement or non-replacement.R 2Be OH, halogen atom, ONa, OK or OR 2a
R 2aBe straight or branched alkyl with 1 to 8 carbon atom or the phenyl of replacement or non-replacement).
Figure S2006800415696D00082
(wherein R represents-A 3-SO 2R 3R 3wAnd R 3XBe halogen atom or hydrogen atom independently of one another.R 3yBe CH 3Base, halogen atom or hydrogen atom.
A 03For replacing or the phenylene of non-replacement or the naphthylidene of replacement or non-replacement.
A 3For replacing or the aromatic ring structure of aliphatic hydrocrbon structure, replacement or the non-replacement of non-replacement or the heterocycle structure of replacement or non-replacement.
R 3Be OH, halogen atom, ONa, OK or OR 3a
R 3aBe straight or branched alkyl with 1 to 8 carbon atom or the phenyl of replacement or non-replacement).
(wherein R represents-A 4-SO 2R 4R 4wAnd R 4XBe halogen atom or hydrogen atom independently of one another.R 4yBe CH 3Base, halogen atom or hydrogen atom.
A 04Phenylene for replacement or non-replacement.This substituting group is to be selected from least a by in the following group of forming: halogen atom, the alkyl with 1 to 20 carbon atom, the alkoxyl group with 1 to 20 carbon atom, OH base, NH 2Base, NO 2Base, COOR 4g(R 4g: H atom, Na atom or K atom one of arbitrarily), acetamido, OPh base, NHPh base, CF 3Base, C 2F 5Base and C 3F 7Base.
A 4For having the straight or branched alkyl of 1 to 8 carbon atom.
R 4Be OH, halogen atom, ONa, OK or OR 4a
R 4aBe straight or branched alkyl with 1 to 8 carbon atom or the phenyl of replacement or non-replacement).
Figure S2006800415696D00101
(R wherein 5wAnd R 5xBe halogen atom or hydrogen atom independently of one another.R 5yBe CH 3Base, halogen atom or hydrogen atom.
A 05Phenylene for replacement or non-replacement.This substituting group is to be selected from least a by in the following group of forming: halogen atom, the alkyl with 1 to 20 carbon atom, the alkoxyl group with 1 to 20 carbon atom, OH base, NH 2Base, NO 2Base, COOR 05g(R 05g: H atom, Na atom or K atom one of arbitrarily), acetamido, OPh base, NHPh base, CF 3Base, C 2F 5Base and C 3F 7Base.Ph represents phenyl (be used for this various).
R 5a, R 5b, R 5c, R 5dAnd R 5eBe SO independently of one another 2R 5f(R 5fBe OH, halogen atom, ONa, OK or OR 5hR 5hExpression has the straight or branched alkyl of 1 to 8 carbon atom or a phenyl of replacement or non-replacement), hydrogen atom, halogen atom, alkyl, alkoxyl group, OH base, NH with 1 to 20 carbon atom with 1 to 20 carbon atom 2Base, NO 2Base, COOR 5g(R 5g: H atom, Na atom or K atom one of arbitrarily), acetamido, OPh base, NHPh base, CF 3Base, C 2F 5Base and C 3F 7Base, condition are R 5a, R 5b, R 5c, R 5dAnd R 5eBe SO one of at least 2R 5f).
Figure S2006800415696D00111
(R wherein 6wAnd R 6xBe halogen atom or hydrogen atom independently of one another.R 6yBe CH 3Base, halogen atom or hydrogen atom.
A 06aPhenylene for replacement or non-replacement.This substituting group is to be selected from least a by in the following group of forming: halogen atom, the alkyl with 1 to 20 carbon atom, the alkoxyl group with 1 to 20 carbon atom, OH base, NH 2Base, NO 2Base, COOR 06ag(R 06ag: H atom, Na atom or K atom one of arbitrarily), acetamido, OPh base, NHPh base, CF 3Base, C 2F 5Base and C 3F 7Base.R 6a, R 6b, R 6c, R 6d, R 6e, R 6fAnd R 6gBe SO independently of one another 2R 6o(R 6oBe OH, halogen atom, ONa, OK or OR 6sR 6sExpression has the straight or branched alkyl of 1 to 8 carbon atom or a phenyl of replacement or non-replacement), hydrogen atom, halogen atom, alkyl, alkoxyl group, OH base, NH with 1 to 20 carbon atom with 1 to 20 carbon atom 2Base, NO 2Base, COOR 6p(R 6p: H atom, Na atom or K atom one of arbitrarily), acetamido, OPh base, NHPh base, CF 3Base, C 2F 5Base and C 3F 7Base, condition are R 6a, R 6b, R 6c, R 6d, R 6e, R 6fAnd R 6gBe SO one of at least 2R 6o).
Figure S2006800415696D00121
(R wherein 6vAnd R 6uBe halogen atom or hydrogen atom independently of one another.R 6zBe CH 3Base, halogen atom or hydrogen atom.
A 06bPhenylene for replacement or non-replacement.This substituting group is to be selected from least a by in the following group of forming: halogen atom, the alkyl with 1 to 20 carbon atom, the alkoxyl group with 1 to 20 carbon atom, OH base, NH 2Base, NO 2Base, COOR 06br(R 06br: H atom, Na atom or K atom one of arbitrarily), acetamido, OPh base, NHPh base, CF 3Base, C 2F 5Base and C 3F 7Base.
R 6h, R 6i, R 6j, R 6k, R 6l, R 6mAnd R 6nBe SO independently of one another 2R 6q(R 6qBe OH, halogen atom, ONa, OK or OR 6tR 6tExpression has the straight or branched alkyl of 1 to 8 carbon atom or a phenyl of replacement or non-replacement), hydrogen atom, halogen atom, alkyl, alkoxyl group, OH base, NH with 1 to 20 carbon atom with 1 to 20 carbon atom 2Base, NO 2Base, COOR 6r(R 6r: H atom, Na atom or K atom one of arbitrarily), acetamido, OPh base, NHPh base, CF 3Base, C 2F 5Base and C 3F 7Base, condition are R 6h, R 6i, R 6j, R 6k, R 6l, R 6mAnd R 6nBe SO one of at least 2R 6q).
(R wherein 7wAnd R 7xBe halogen atom or hydrogen atom independently of one another.R 7yBe CH 3Base, halogen atom or hydrogen atom.R 7aBe OH, halogen atom, ONa, OK or OR 7b
R 7bBe straight or branched alkyl with 1 to 8 carbon atom or the phenyl of replacement or non-replacement).
(R wherein 8wAnd R 8xBe halogen atom or hydrogen atom independently of one another.R 8yBe CH 3Base, halogen atom or hydrogen atom.R 8aBe OH, halogen atom, ONa, OK or OR 8b
R 8bBe straight or branched alkyl with 1 to 8 carbon atom or the phenyl of replacement or non-replacement).
Figure S2006800415696D00141
(R wherein 9wAnd R 9xBe halogen atom or hydrogen atom independently of one another.R 9yBe CH 3Base, halogen atom or hydrogen atom.
R 9aBe OH, halogen atom, ONa, OK or OR 9b
R 9bBe straight or branched alkyl with 1 to 8 carbon atom or the phenyl of replacement or non-replacement).
Figure S2006800415696D00151
(R wherein 10wAnd R 10xBe halogen atom or hydrogen atom independently of one another.R 10yBe CH 3Base, halogen atom or hydrogen atom.R 10aBe OH, halogen atom, ONa, OK or OR 10b).
R 10bBe straight or branched alkyl with 1 to 8 carbon atom or the phenyl of replacement or non-replacement).
Figure S2006800415696D00152
(R wherein 11wAnd R 11xBe halogen atom or hydrogen atom independently of one another.R 11yBe CH 3Base, halogen atom or hydrogen atom.R 11aBe OH, halogen atom, ONa, OK or OR 11b
R 11bBe straight or branched alkyl with 1 to 8 carbon atom or the phenyl of replacement or non-replacement).
Polymkeric substance of the present invention can be multipolymer, the unit that this multipolymer also comprises at least one derived from ethylene base class monomer and represented by chemical formula (101) except comprising the arbitrary unit by chemical formula (1) to (11) expression.
Figure S2006800415696D00161
(R wherein 101wAnd R 101xBe halogen atom or hydrogen atom independently of one another.R 101yBe CH 3Base, halogen atom or hydrogen atom.
R 101For the heterocycle structure of aromatic ring structure, replacement or the non-replacement of aliphatic hydrocrbon structure, replacement or the non-replacement of hydrogen atom, replacement or non-replacement, halogen atom ,-CO-R 101a,-O-R 101b,-COO-R 101c,-OCO-R 101d,-CONR 101eR 101f,-CN or contain the ring structure of N atom.R 101a, R 101b, R 101c, R 101d, R 101eAnd R 101fBe the aromatic ring structure of aliphatic hydrocrbon structure, replacement or non-replacement of hydrogen atom, replacement or non-replacement or the heterocycle structure of replacement or non-replacement independently of one another).
At this, in the present invention, have by the unit in the unitary multipolymer of chemical formula (1) expression and derived from ethylene base class monomer and be 0.1 to 100mol% by the unitary ratio of chemical formula (101) expression, more preferably 1.0 to 50mol%, in the unitary content of being represented by chemical formula (1).
(weight-average molecular weight/number-average molecular weight=Mw/Mn) can be 1＜Mw/Mn＜10 preferably shows as 1＜Mw/Mn＜2 to the molecular weight distribution of polymkeric substance of the present invention.
Comprise of the present invention by chemical formula (1) to (11) expression arbitrary unit and derived from ethylene base class monomer and can be segmented copolymer by the unitary multipolymer of chemical formula (101) expression.The number-average molecular weight of preferred polymkeric substance of the present invention is 1000 to 1000000.
Can be used as the monomeric compound that is used for production polymkeric substance of the present invention and comprise the compound that has by the structure of chemical formula (201) expression.
Figure S2006800415696D00171
(wherein R represents-A 201-SO 2R 201R 201wAnd R 201XBe halogen atom or hydrogen atom independently of one another.R 201yBe CH 3Base, halogen atom or hydrogen atom.
A 0201For replacing or the aromatic ring structure of non-replacement or the heterocycle structure of replacement or non-replacement.
A 201For replacing or the aromatic ring structure of aliphatic hydrocrbon structure, replacement or the non-replacement of non-replacement or the heterocycle structure of replacement or non-replacement.
R 201Be OH, halogen atom, ONa, OK or OR 201a
R 201aFor replacing or the aromatic ring structure of aliphatic hydrocrbon structure, replacement or the non-replacement of non-replacement or the heterocycle structure of replacement or non-replacement).
Can be used as the monomeric compound that is used for production polymkeric substance of the present invention and comprise the compound that has by the structure of chemical formula (202) expression.
Figure S2006800415696D00172
(wherein R represents-A 202-SO 2R 202R 202wAnd R 202XBe halogen atom or hydrogen atom independently of one another.R 202yBe CH 3Base, halogen atom or hydrogen atom.
A 0202For replacing or the aromatic ring structure of non-replacement or the heterocycle structure of replacement or non-replacement.
A 202For replacing or the aromatic ring structure of aliphatic hydrocrbon structure, replacement or the non-replacement of non-replacement or the heterocycle structure of replacement or non-replacement.R 202Be OH, halogen atom, ONa, OK or OR 202aR 202aBe methyl, ethyl or phenyl).
(production method)
Can produce the above-mentioned unitary polymkeric substance that comprises by chemical formula (1) expression by at least a compound of polymerization by chemical formula (201) expression.
In addition, can obtain the unitary polymkeric substance that comprises by chemical formula (1) expression of the present invention by making to comprise the unitary polymkeric substance of representing by chemical formula (301) and carry out condensation reaction by at least a amine compound that chemical formula (302) is represented.
In the production method of the unitary polymkeric substance that comprises the expression of chemical formula (1) thus, preferably use condensing agent in same reacting field, to form amido linkage.As the condensing agent that is used for this purpose, can use phosphoric acid class condensing agent.In addition, can further in the presence of pyridine, carry out this condensation reaction.
In addition, the unitary polymkeric substance that comprises by chemical formula (304) expression of the present invention can obtain by the unitary polymkeric substance that uses the esterifying agent esterification to comprise by chemical formula (303) expression.
The above-mentioned esterifying agent that adopts in the production method that comprises the unitary polymkeric substance of being represented by above-mentioned chemical formula (304) comprises trimethyl silyl diazomethane, trimethyl orthoformate, triethyl orthoformate, tributyl orthoformate or tripropyl orthoformate.
(charge control agent)
The electriferous state of charge control agent control fine particle of the present invention, and it is characterized in that comprising to have the unitary polymkeric substance of structure by chemical formula (1) expression.
Further preferred above-mentioned granulated material is the toning agent that is used for developing electrostatic latent image.
And the unit by chemical formula (1) expression as the polymkeric substance that constitutes charge control agent can use the unit by chemical formula (2) to (11) expression.
(polymkeric substance of the present invention is production method more specifically)
Below, will describe the present invention in detail by preferred embodiment.Have above-mentioned each polymkeric substance of the present invention that constitutes and have utmost point excellent characteristic as charge control agent.In addition, comprise the toning agent that is used for developing electrostatic latent image of the charge control agent that uses this polymkeric substance, when at first using it for image forming apparatus, have significant effect with the toning system by electrofax.Can enumerate the production method of following method as this polymkeric substance.
For example, by having the unitary polymkeric substance of representing by chemical formula (1) as the unitary polymkeric substance and at least a production that have by chemical formula (301) expression that raw material uses by the reaction between the compound of chemical formula (302) expression.
In this method, be used as raw material by having by the unit of chemical formula (301) expression and the polymkeric substance of molecular weight distribution 1＜Mw/Mn＜2, can synthesize the unit and the polymkeric substance of molecular weight distribution in above-mentioned scope that have by chemical formula (1) expression.
Also can be used as raw material with comprising by the unit of chemical formula (301) expression with by the monomeric unitary segmented copolymer of derived from ethylene base class that chemical formula (101) is represented.In the case, can synthesize and comprise by the unit of chemical formula (1) expression with by the monomeric unitary segmented copolymer of derived from ethylene base class of chemical formula (101) expression.(comprising production method) by the unitary polymkeric substance of chemical formula (301) expression
Use known polymerization process and polymer reaction, can be multipolymer with the polymer production with carboxyl by chemical formula (301) expression, this multipolymer also has the vinyl monomer unit by chemical formula (101) expression except that the unit with chemical formula (301).
As the unitary vinyl monomer that is used for introducing by chemical formula (101) expression, can mention various following compounds.
Vinylbenzene and derivative thereof, the unsaturated monoolefine of olefinic, halogen ethene, vinyl ester, alpha-methylene aliphatic monocarboxylic acid ester, vinyl ether, acrylic or methacrylic acid derivative.
Can obtain having the unitary polymkeric substance of vinyl benzoic acid as following.
For polymkeric substance with carboxyl by chemical formula (301) expression; in the carboxylic acid of vinyl benzoic acid, introduce protecting group with synthon; and after its polymerization, remove protecting group to obtain the having unitary polymkeric substance of vinyl benzoic acid by carrying out polymer reaction.
Have by the unit of chemical formula (301) expression and the polymkeric substance of molecular weight distribution 1.00＜Mw/Mn＜2.00 and can synthesize by using living polymerisation process.
As active free radical polymerization, for example following explanation atom transfer radical polymerization and nitrogen oxygen regulation and control polymerization (nitroxide mediated polymerization).
At first, illustrate that wherein active free radical polymerization is the situation of atom transfer radical polymerization.
According to atom transfer radical polymerization, by quick shift reaction, for example by using copper halide-dipyridyl title complex can obtain having the polymkeric substance of narrow molecular weight distributions at the polymer chain end.
As reaction solvent, can use for example dimethyl sulfoxide (DMSO), dimethyl formamide etc.
Secondly, illustrate that wherein active free radical polymerization is nitrogen oxygen regulation and control polymeric situation.
2,2,6,6-tetramethyl piperidine (TEMPO), it is a kind of of nitroxyl free radical, and unpaired electron delocalization wherein, it provides the free radical bonding of low ionic dissociation energy when being difficult to bonding.Utilize this specific character, use benzoyl peroxide (BPO) and Diisopropyl azodicarboxylate (AIBN), regulate and control the polymkeric substance that polymerization can obtain having narrow molecular weight distributions by the nitrogen oxygen that uses the nitroxyl free radical as initiator.
Polymerisable monomer, initiator and nitroxyl free radical are added in the reaction solvent, and reaction system is with inert gas replacement and carry out nitrogen oxygen regulation and control polymerization.
For the nitroxyl free radical, can use those that for example describe below.
Figure DEST_PATH_G200680041569601D00011
Nitroxyl free radical 1 (TEMPO)
For reaction solvent, for example can use for example dimethyl sulfoxide (DMSO), dimethyl formamide etc.
Comprise by the unit of chemical formula (301) expression and the monomeric unitary segmented copolymer of representing by chemical formula (101) of derived from ethylene base class by using the living polymerisation process in the known polymerization process, can synthesizing.In living polymerisation process, active free radical polymerization is especially relatively easy.
Particularly, after forming homopolymer,, make polymkeric substance be copolymerized to an end of this homopolymer with structure of representing by chemical formula (101) by active free radical polymerization with structure of representing by chemical formula (301) by active free radical polymerization.In this way can obtain the precursor of target segmented copolymer.
The order that forms segmented copolymer can be opposite.
The preferred atom transfer radical polymerization of active free radical polymerization and nitrogen oxygen regulation and control polymerization, its can with have mode identical under the unitary polymkeric substance situation of chemical formula (301) and carry out above-mentioned.
(by the compound of chemical formula (302) expression)
Be used for the compound by chemical formula (302) expression of the present invention and can be wherein A 302Be following compound.
That is, this compound can be wherein A 302Be following compound: have 1 to 8 carbon atom straight or branched alkylidene group, replacement or non-replacement phenyl, replacement or non-replacement naphthyl or comprise any one or the multiple replacement or the heterocycle structure of non-replacement of N, S and O.
Work as A 302During for ring structure, non-substituted ring can be further and its condensation.
A wherein 302For the specific examples of the compound of straight or branched alkylidene group with 1 to 8 carbon atom comprises following.That is, 2-aminoethane sulphonic acid (taurine), 3-amino propane sulfonic acid, 4-aminobutane sulfonic acid, 2-amino-2-methyl propane sulfonic acid and an alkali metal salt thereof.
A wherein 302For replacing or the compound of the phenyl of non-replacement is represented by chemical formula (26).
Figure S2006800415696D00221
(R wherein 26a, R 26b, R 26c, R 26dAnd R 26eRepresent SO independently of one another 2R 26f(R 26fBe OH, halogen atom, ONa, OK or OR 26hR 26hThe aromatic ring structure of aliphatic hydrocrbon structure, replacement or the non-replacement of expression replacement or non-replacement or the heterocycle structure of replacement or non-replacement.), hydrogen atom, halogen atom, alkyl, alkoxyl group, OH base, NH with 1 to 20 carbon atom with 1 to 20 carbon atom 2Base, NO 2Base, COOR 26g(R 26gExpression H atom, Na atom and K atom one of any.), acetamido, OPh base, NHPh base, CF 3Base, C 2F 5Base or C 3F 7Base, and R wherein 26a, R 26b, R 26c, R 26dAnd R 26eBe SO one of at least 2R 26f).
Compound by chemical formula (26) expression comprises various amino phenyl sulfonyl acid derivatives and salt thereof, as Sulphanilic Acid (sulfanilic acid).In addition, it also comprises methyl-esterified compound or phenylester compound such as the 2-aniline sulfonic acid methyl ester of esterification compound such as various amino phenyl sulfonyl acid derivatives.
A wherein 27For replacing or the compound of the naphthyl of non-replacement is represented by chemical formula (27a) with (27b).
Figure S2006800415696D00231
(R wherein 27a, R 27b, R 27c, R 27d, R 27e, R 27fAnd R 27gRepresent SO independently of one another 2R 27o(R 27oBe OH, halogen atom, ONa, OK or OR 27sR 27sThe aromatic ring structure of aliphatic hydrocrbon structure, replacement or the non-replacement of expression replacement or non-replacement or the heterocycle structure of replacement or non-replacement.), hydrogen atom, halogen atom, alkyl, alkoxyl group, OH base, NH with 1 to 20 carbon atom with 1 to 20 carbon atom 2Base, NO 2Base, COOR 27p(R 27pExpression H atom, Na atom and K atom one of any.), acetamido, OPh base, NHPh base, CF 3Base, C 2F 5Base or C 3F 7Base, and R wherein 27a, R 27b, R 27c, R 27d, R 27e, R 27fAnd R 27gBe one of at least SO independently separately 2R 27o).
Figure S2006800415696D00232
(R wherein 27h, R 27i, R 27j, R 27k, R 27l, R 27mAnd R 27nRepresent SO independently of one another 2R 27q(R 27qBe OH, halogen atom, ONa, OK or OR 27tR 27tThe aromatic ring structure of aliphatic hydrocrbon structure, replacement or the non-replacement of expression replacement or non-replacement or the heterocycle structure of replacement or non-replacement.), hydrogen atom, halogen atom, alkyl, alkoxyl group, OH base, NH with 1 to 20 carbon atom with 1 to 20 carbon atom 2Base, NO 2Base, COOR 27r(R 27rExpression H atom, Na atom and K atom one of any.), acetamido, OPh base, NHPh base, CF 3Base, C 2F 5Base or C 3F 7Base, and R wherein 27h, R 27i, R 27j, R 27k, R 27l, R 27mAnd R 27nBe SO one of at least 2R 27q).
By chemical formula (27a) or (27b) expression compound comprise various ALPHA-NAPHTHYL AMINE sulfonic acids and salt such as 1-ALPHA-NAPHTHYL AMINE-4-sulfonic acid.In addition, it also comprises methyl-esterified compound or the phenylester compound such as the 1-ALPHA-NAPHTHYL AMINE-8-sulfonic acid methyl ester of esterification compound such as various ALPHA-NAPHTHYL AMINE sulfonic acids.
A wherein 302For comprise N, S and O one or more replacement or the compound of the heterocycle structure of non-replacement comprise pyridine ring, piperazine ring, furan nucleus and mercaptan ring.(production method that in molecule, has one or more unitary polymkeric substance by chemical formula (1) expression)
Specifically describe and comprise in the present invention by the unitary polymkeric substance of chemical formula (301) expression with by the condensation reaction between the sulfamic acid compound of chemical formula (302) expression.
For the condensation reaction between carboxyl and the amino, can adopt any means, as the method for using condensing agent, form salt and carry out the method for condensation and use the method for dewatering agent by dehydration reaction.
Detailed description is as the method for the use condensing agent of production method of the present invention.As condensing agent, can use phosphoric acid class condensing agent.In reaction of the present invention, preferably use phosphoric acid ester (phosphate-based) condensing agent.As the phosphorous acid ester that is used for this purpose (phosohites), preferably use triphenyl phosphite.In the scope of the amount of the condensing agent that uses more than 0.1mol, preferably equate the scope that mol is above, based on the compound of every mol by chemical formula (302) expression.Condensing agent itself also can be used as reaction solvent.
To use in present method by the amount of the compound of chemical formula (302) expression in 0.1 to 50.0mol scope, preferred 1.0 to 20.0mol, will be as the unit by chemical formula (301) expression of raw material based on every mol.In reaction of the present invention, if necessary, can use solvent.Pyridine is suitable for as the solvent that will use.
In the method for the invention, for example, the reaction times is in 1 to 48 hour scope.Be included in have in the molecule one or more by chemical formula (1) expression and produce in this way the reaction solution of unitary polymkeric substance can remove for the distillation of ordinary method by it.
Use solvent such as ether with this reaction solution with to this reaction solution for evenly solvable and be insoluble solvent in molecule, having one or more unitary polymkeric substance by chemical formula (1) expression.Then, make in molecule, to have one or more unitary polymkeric substance redeposition by chemical formula (1) expression, and with its collection.
If desired, separable and purifying obtains thus has one or more unitary polymkeric substance by chemical formula (1) expression in molecule.Method to separation and purifying is not particularly limited, and can adopt use is that insoluble solvent is with the method for precipitation polymers and the method for use column chromatography to have one or more unitary polymkeric substance by chemical formula (1) expression in molecule.
When will be wherein molecular weight distribution be 1.00＜Mw/Mn＜2.00 have unitary polymkeric substance by chemical formula (301) expression as raw material the time, can carry out condensation reaction by identical method.
When comprising by the unit of chemical formula (301) expression with by the monomeric unitary segmented copolymer of derived from ethylene base class of chemical formula (101) expression during as raw material, this condensation reaction also can be undertaken by identical method.
It can also synthesize by using compound, another polymerisable monomer and the polymerization starter represented by chemical formula (201) to carry out copolymerization.
(by the production method of the compound of chemical formula (201) expression)
Compound by chemical formula (201) expression can be by following method production.
Describe the synthetic method of the compound of representing by chemical formula (201) among the present invention in detail.Its polymerisable monomer by having carboxyl as vinyl benzoic acid, wherein the carboxyl chloride of acid polymerisable monomer that is converted into chloride of acid (acid chloride) with synthesize by the various condensation reactions of chemical formula (401) expression as described in following with amino compound.
For the condensation reaction between carboxyl and the amino; can adopt any means; as use condensing agent method, form salt and carry out the method for condensation and use the method for dewatering agent by dehydration reaction, and carboxyl is converted into chloride of acid and makes itself and the method for amino reaction.
Carboxyl is converted into chloride of acid and its method with amino reaction is described in detail as production method of the present invention.
By using thionyl chloride can carry out by the conversion to chloride of acid of the polymerisable monomer of chemical formula (203) expression, it is an ordinary method.
(R wherein 203wAnd R 203XBe halogen atom or hydrogen atom independently of one another.R 203yBe CH 3Base, halogen atom or hydrogen atom.
A 0203For replacing or the heterocycle structure of the aromatic ring structure of non-replacement or replacement or non-replacement one of any.R 203Be H atom, Na atom or K atom).
The amount of the thionyl chloride of using is in 0.1 to 50.0mol scope, and preferred 1.0 to 20.0mol, based on the compound of every mol by chemical formula (203) expression.Thionyl chloride itself also can be used as reaction solvent.
To use in present method by the amount of the compound of following chemical formula (401) expression in 0.1 to 50.0mol scope, preferred 1.0 to 20.0mol, will be as the unit by chemical formula (203) expression of raw material based on every mol.In reaction of the present invention, if necessary, can use solvent.The solvent that uses comprises methylene dichloride, chloroform, tetracol phenixin, ethylene dichloride, trichloroethane etc.In this method, temperature of reaction does not limit especially, but it typically is-30 ℃ of temperature to the scope of solvent boiling point.Yet, preferably under the optimum temps of compound that is suitable for most representing and reaction solvent, carry out this reaction by following chemical formula (401).In the method for the invention, the reaction times does not generally limit, but usually in 1 to 48 hour scope.The consequent reaction solution that comprises the compound of being represented by chemical formula (201) can be removed for the distillation of ordinary method by it.
If desired, the compound that obtains thus of separable and purifying by chemical formula (201) expression.This separation and purification process are not particularly limited, can adopt use to by the solvent of the compound indissoluble of chemical formula (201) expression with the method for recrystallization and the method by column chromatography.
In compound, can synthesize by aforesaid method and not have the unitary compound of sulphonate by chemical formula (201) expression.
For example, as synthetic wherein R 201During for the compound of OH, halogen atom, ONa, OK, can synthesize wherein R by further use esterifying agent 201By OR 201aExpression have a unitary compound of sulphonate by chemical formula (201) expression.This esterifying agent comprises trimethyl silyl diazomethane, trimethyl orthoformate, triethyl orthoformate etc.
In this reaction, if necessary can use aforementioned solvents.
The amount of the esterifying agent of using is in 0.1 to 50mol scope, and preferred 1 to 20mol, based on every mole of unit by chemical formula (201) expression, R in this chemical formula 201Be OH, halogen atom, ONa, OK.
In this method, temperature of reaction does not limit especially, but it typically is the temperature in-20 ℃ to 200 ℃ scopes.Reaction times does not generally limit, but usually in 1 to 48 hour scope.
Consequent reaction solution can be removed for the distillation of ordinary method by it, and this reaction solution comprises and has the unitary wherein R of sulphonate 201Represent OR 201aThe compound by chemical formula (201) expression.
If necessary, can separate and purifying obtains thus and has a unitary wherein R of sulphonate 201By OR 201aThe compound by chemical formula (201) expression of expression.This separation and purification process are not particularly limited, can adopt use in chemical formula (201), having sulphonate unit and R wherein 201By OR 201aThe solvent of the compound indissoluble of expression is with the method for recrystallization and the method by column chromatography.(by the compound of chemical formula (401) expression)
H 2N-A 401-SO 2R 401 (401)
(R wherein 401Be OH, halogen atom, ONa, OK or OR 401aR 401aIndependently of one another for replacing or the aromatic ring structure of aliphatic hydrocrbon structure, replacement or the non-replacement of non-replacement or the heterocycle structure of replacement or non-replacement).
Be used for the present invention by the compound of chemical formula (401) expression preferably below.
That is A wherein, 401For the naphthyl of phenyl, replacement or the non-replacement of straight or branched alkylidene group, replacement or non-replacement with 1 to 8 carbon atom or comprise N, S and O one or more replacement or the compound of the heterocycle structure of non-replacement.Work as A 401During for ring structure, the further non-substituted ring of condensation.
Work as A 401When having the straight or branched alkylidene group of 1 to 8 carbon atom, this examples for compounds comprises following.That is, 2-aminoethane sulphonic acid (taurine), 3-amino propane sulfonic acid, 4-aminobutane sulfonic acid, 2-amino-2-methyl propane sulfonic acid and an alkali metal salt thereof.
Work as A 401For replacing or during the phenyl of non-replacement, it is represented by above-mentioned chemical formula (26).
Work as A 401For replacing or during the naphthyl of non-replacement, it is by above-mentioned chemical formula (27a) or (27b) expression.
Work as A 401For comprise N, S and O one or more replacement or during the heterocycle structure of non-replacement, it comprises pyridine ring, piperazine ring, furan nucleus and mercaptan ring.(by the polymerization process of the compound of chemical formula (201) expression)
Polymerization process as the compound of being represented by chemical formula (201) can adopt various known polyreactions.Also can carry out this compound and various known monomeric copolymerization.
Can be comprised vinylbenzene, o-methyl styrene by the monomeric example of copolymerization.
In being aggregated in chemical formula (201), do not have the unitary compound of sulphonate (for example, R wherein 617Compound for OH, halogen atom, ONa, OK) time, can adopt the radical polymerization of relatively easy controlled polymerization condition.
Simultaneously, when compound has the sulphonate unit, can adopt ionic polymerization.
When using radical polymerization fashionable, initiator for example comprises 2,2 '-Diisopropyl azodicarboxylate.In addition, can adopt water soluble starter such as Potassium Persulphate, ammonium persulphate.
These can be used alone or in combination.Its consumption but can suitably be determined according to the monomeric species that will use, the monomer that will be used for copolymerization, the initiator that will use preferably in the total polymerisable monomer of every mol is 0.0001 to 0.5mol scope.
In polyreaction of the present invention, if necessary can use aforementioned solvents, toluene and N, dinethylformamide.
In addition, wherein molecular weight distribution is that having of 1.00＜Mw/Mn＜2.00 can be synthetic by the living polymerisation process in the known polymerization process of special use by the unitary polymkeric substance of chemical formula (1) expression.In this living polymerisation process, active free radical polymerization is relatively easy.This active free radical polymerization, preferred atom transfer radical polymerization and nitrogen oxygen regulation and control polymerization can be to carry out with mode identical under the situation of above-mentioned unitary polymkeric substance with chemical formula (301).
Living polymerisation process in the polymerization process of knowing by special use can also synthesize and comprises by the unit of chemical formula (1) expression with by the monomeric unitary segmented copolymer of derived from ethylene base class of chemical formula (101) expression.
In this living polymerisation process, active free radical polymerization is relatively easy.
Particularly, after forming homopolymer, make polymkeric substance be copolymerized to an end of this homopolymer with structure of representing by chemical formula (101) by active free radical polymerization with structure of representing by chemical formula (301) by active free radical polymerization.In this way can obtain the precursor of target segmented copolymer.
The order that forms segmented copolymer can be opposite.Can also with the situation of above-mentioned unitary polymkeric substance with chemical formula (301) under, identical mode is carried out this active free radical polymerization.
Can remove solvent in the consequent reaction solution that comprises polymkeric substance of the present invention for the distillation of ordinary method by it.Perhaps, will be that for example water, alcohol make the polymer precipitation as target of the present invention as methyl alcohol and ethanol or ether and this reaction solution uniform mixing to insoluble solvent for polymkeric substance of the present invention.Collecting precipitation.This ether comprises for example dimethyl ether, Anaesthetie Ether, tetrahydrofuran (THF).
If necessary, can separate and the polymkeric substance of the present invention that obtains thus of purifying.This separation and purification process are not particularly limited, can adopt use to the solvent of polymkeric substance indissoluble of the present invention with sedimentary method and the method by column chromatography.(production method that in molecule, has one or more unitary polymkeric substance by chemical formula (304) expression)
R in chemical formula (303) 1During for OH, halogen atom, ONa or OK, can by use esterifying agent synthetic by R wherein by-A 304-SO 3R 304The polymkeric substance of chemical formula (304) expression of expression.For example, this esterifying agent is trimethyl silyl diazomethane, trimethyl orthoformate, triethyl orthoformate.
Below describe this reaction in detail.
In this reaction, if necessary can use above-mentioned or following solvents.Preferred chloroform, the methyl alcohol of using.The amount of the solvent of using can suitably be determined according to raw material, reaction conditions etc.
The amount of the esterifying agent that uses is in 0.1 to 50mol scope, and preferred 1 to 20mol, based on the unit of every mol by chemical formula (303) expression.
In this method, temperature of reaction does not limit especially, but it typically is the temperature in-20 ℃ to 200 ℃ scopes.Reaction times does not generally limit, but usually in 1 to 48 hour scope.
Can remove solvent in the consequent reaction solution that comprises polymkeric substance of the present invention for the distillation of ordinary method by it.
(being applied to toning agent)
The purposes of polymkeric substance of the present invention comprises the image forming method that is applied in the toning agent that is used for developing electrostatic latent image and uses this toning agent.
Particularly, it can be used as Nei Jia or is added on charge control agent in the toning agent outward.In other words, the present invention relates to comprise the charge control agent of above-mentioned polymkeric substance, and the toning agent that is used for developing electrostatic latent image that comprises this charge control agent in addition.
As the charge control agent that will be used for the toner for developing electrostatic latent image composition, can provide static characteristic, compound dispersiveness and the cost excellent electric charge control agent in toner resin by using the polymer compound of for example representing by chemical formula (1).
Image hazes and shows the toning agent that is used for developing electrostatic latent image of good transfer printing when in addition, using polymkeric substance of the present invention to provide to be reduced in image forming apparatus output.
And, can make charge control agent of the present invention be colourless or weak painted, therefore, can select any tinting material and not be subjected to the influence of charge control agent according to the form and aspect that color toner requires.The original form and aspect that colourless or weak painted charge control agent hinders dyestuff or pigment to have hardly, and be preferred.
＜as charge control agent 〉
When with polymkeric substance of the present invention when the charge control agent, preferably its side chain has the sulfonic group of comprising or derivatives thereof, as the structure by the monomeric unit of above-mentioned chemical formula (1) expression.Unitary existence with negatively charged ion or electrophilic functional group shows good negative charging.
The resin glue of polymkeric substance of the present invention and toning agent has good consistency, especially has fabulous consistency with polyester binder resin.
Owing to comprise the satisfactory stability that polymkeric substance toning agent of the present invention has the height ratio quantity of electric charge (specific charge quantity) and passs in time, even after this toning agent standing storage, it stably provides clear image in also forming at the image of electrostatic recording.In addition, it is for colourless or weak painted and have good electronegative property, can be made into that black can electronegative toning agent and color toner arbitrarily.And, constitute the type/ratio of components of the monomeric unit of polymkeric substance of the present invention by suitable selection, can wide region control consistency.
So that charge control agent when having micro phase separation structure in toner adhesive, suppresses the electric continuity (electriccontinuity) of toning agent, can stablize the maintenance electric charge when selecting resin combination.
(polymkeric substance of the present invention is added in the toning agent)
Make in the present invention toning agent comprise the method for the charge control agent that contains above-mentioned polymkeric substance comprise with add in it in toning agent method and with its outer method that adds in the toning agent.The add-on of charge control agent is usually at 0.1 to 50 quality %, in preferred 0.2 to the 20 quality % scope, with respect to the total mass of toner adhesive and charge control agent under interior situation about adding.When it is lower than 0.1 quality %, may not significantly observe the improvement degree of toning agent charging property.On the other hand, when it surpasses 50 quality %, be preferred situation from the viewpoint of economy.Mass ratio for toner adhesive under situation about adding and charge control agent, the add-on of charge control agent is preferably in the scope of 0.01 to 5 quality %, with respect to the total mass of toner adhesive and charge control agent, especially preferred charge control agent mechanochemistry adheres to toner surface (mechnochemically).
The molecular weight of polymkeric substance of the present invention is measured by GPC (gel permeation chromatography).The above-mentioned polymkeric substance of preferred in the present invention use, the ratio (Mw/Mn) of weight-average molecular weight of wherein as above measuring when it is used as charge control agent (Mw) and number-average molecular weight (Mn) is in 1 to 10 scope.
For the particle size range of the discontinuous magnetic domain that reduces polymer formation of the present invention, can comprise with polymkeric substance of the present invention and have consistency and have the polymkeric substance of consistency as compatibility agent with toner adhesive.This compatibility agent comprises following.
For example, it is following polymkeric substance, comprises the polymer of monomers chain and the polymer of monomers chain bonding that has and constitute the basic identical structure of monomer of toner adhesive that comprises more than the 50mol% that have and constitute the basic identical structure of monomer of polymkeric substance of the present invention more than the 50mol% in this polymkeric substance.
For the form of bonding, it can connect with the form of grafting or block.
Will with the amount of compatibility agent be generally below the 30 quality %, be preferably 1 to 10 quality %, based on polymkeric substance of the present invention.
The ordinary hot plastic resin can be used as resin glue and is used for toning agent of the present invention.The example comprises polystyrene.
When forming the resin glue that will be used in combination with charge control agent of the present invention, if necessary can use linking agent given below.Bifunctional cross-linker's example comprises Vinylstyrene.
When forming the resin glue that will be used in combination with charge control agent of the present invention, if necessary can use polymerization starter given below.The example comprises tert-butyl peroxide-2-ethyl hexanoate.
Except that charge control agent of the present invention, the conventional charge control agent that uses can be used in combination with charge control agent of the present invention.
As constituting according to the tinting material that is used for the toning agent of developing electrostatic latent image of the present invention, can use any tinting material, as long as it is generally used for producing toning agent, and to its qualification especially.And, from the viewpoint of full color images (full color image) quality, preferably dyestuff and pigment combinations are used to improve purity.Usually, in order to obtain best toning agent characteristic, in other words, consider the dispersing of shape stability, toning agent of tinting strength, the toning agent in when printing, tinting material is to be 0.1 to 60 mass parts with respect to 100 mass parts resin glues, and the ratio of preferred 0.5 to 20 mass parts is used.
Except that above-mentioned resin glue and coloring agent component, the toning agent that is used for developing electrostatic latent image according to the present invention can comprise following compounds with the scope of not destroying effect of the present invention.For example, it is a silicone resin.
Any conventional currently known methods can be used as be used to prepare have above-mentioned formation according to the concrete grammar that is used for the toning agent of developing electrostatic latent image of the present invention.
In the present invention, preferably fine silica is added to outward by in the toning agent of aforesaid method manufacturing to improve stability, developing property, flowability and weather resistance.
In addition, the inorganic powder that provides below preferred the adding is to improve the developing property and the weather resistance of toning agent.For example, it preferably uses zinc oxide, aluminum oxide, cobalt oxide, Manganse Dioxide, strontium titanate and magnesium titanate fine powder.And slip additive (slippering additive) powder such as teflon (Teflon) can add in the toning agent.
＜about carrier 〉
The toning agent that is used for developing electrostatic latent image according to the present invention can be applicable to the known toning agent of various routines.For example, the toning agent itself that is used for developing electrostatic latent image can be used as the photographic developer that is used for non-magnetic monocomponent toner.The toning agent that is used for developing electrostatic latent image according to the present invention can be used as with using the magnetic carrier of the toning agent that acts on magnetic mono-component toner or the nonmagnetic toner that magnetic color tuner constitutes the magnetic two-component developing agent independently.
＜magnetic color tuner 〉
The toning agent that is used for developing electrostatic latent image according to the present invention can be made magnetic color tuner by making magneticsubstance be included in toner particle.In this case, this magneticsubstance also can serve as tinting material.With respect to the magneticsubstance that can be used among the present invention, below the preferred 2 μ m of median size, 0.1 to 0.5 μ m more preferably from about.Be included in preferred 20 to 200 mass parts of amount in the toning agent, for 100 mass parts resin glues, more preferably 40 to 150 mass parts are based on 100 mass parts resin glues.
And, be necessary to make its littler latent image dots of can verily developing to reach high resolving power, therefore, for example preferably adjust, so that it is in the scope of 4 μ m to 9 μ m according to the weight average particle diameter that is used for the toner particle of developing electrostatic latent image of the present invention.Have toner particle that weight average particle diameter is lower than 4 μ m and cause that transfer efficiency reduces and is tending towards residual transfer printing toning agent not in a large number on photoreceptor, it causes based on hazing and the image of transfer printing defective uneven irregular, is not preferred.Simultaneously, when the weight average particle diameter of toner particle during, be tending towards occurring dispersing of literal and line image greater than 9 μ m.
In the present invention, Coulter counter TA-II type or Coultermulti-sizers (being made by Beckman Coulter Corporation) are used to measure the median size and the size distribution of toning agent.
In addition, the toning agent that is used for developing electrostatic latent image according to the present invention has the preferred electric charge of per unit mass (two-pack method) at-10 to-80 μ C/g, more preferably-15 to-70 μ C/g, this is because can improve transfer efficiency in the printing transferring method of the transfer member that working voltage is applied thereto.
The method of measuring carried charge by the two-pack method of using among the present invention below is shown.The charge analysis equipment that is shown in Fig. 5 is used for this measurement.At first, preparation wherein is added to the EFV200/300 (by Powder Tech Corporation made) of 9.5g as carrier with 0.5g as the toning agent of measuring object))) mixture.This mixture put into the bottle of the volume of being made by polyethylene 50 to 100ml, and be installed to and have uniform amplitude, vibration condition is on 100mm amplitude and 100 reciprocating shaking machines of per minute, and bottle is shaken certain hour.Then 1.0 to 1.2g said mixtures are placed on the metal measuring vessel 42 with sieve 43, this sieve 43 is 500 orders, is positioned at the bottom of the coulometry equipment 41 that is shown in Fig. 5 and uses metal lid 44 to cover.The quality representation of whole measuring vessel 42 is scale W1 (g) with this moment.Aspirate from pump orifice 47 by unshowned suction machine (part that contacts with measuring vessel 42 is an isolator at least) then, so that make the pressure at vacuumometer 45 places can become 2450Pa (250mmAq) by regulating air control valve 46.By suction under this state 1 minute with toning agent suction and remove.The current potential at potentiometer 49 places is expressed as V (Volt) with this moment.At this, Reference numeral 48 is represented electric capacity and electrical capacity is expressed as C (μ F).The quality representation of whole measuring vessel is scale W2 (g) with this moment.Calculate the frictional electrification amount (μ C/g) of toning agent by following formula by these observed values.
Calculation formula: frictional electrification amount (μ C/g)=C * V/ (W1-W2)
These operate under the controlled condition and carry out (for example it carries out) under steady temperature and humidity conditions.
The molecule measuring metering method and the molecular weight distribution of＜resin glue 〉
Particularly when preparing, be used for the resin glue that the constituent material that is used for the toning agent of developing electrostatic latent image according to the present invention uses and preferably have the peak by the lower molecular weight zone in molecular weight distribution 3,000 to 15,000 scopes of GPC by breaking method.That is, the GPC peak in the lower molecular weight zone surpasses at 15,000 o'clock, may be difficult to obtain transfer efficiency fully improved those.Being lower than when resin glue when having the GPC peak in 3,000 the lower molecular weight scope, being tending towards bonding occurring when surface treatment, is not preferred.
In the present invention, the molecular weight of resin glue is measured by GPC (gel permeation chromatography).As concrete gpc measurement method, in advance toning agent is used apparatus,Soxhlet's (Soxhlet) with THF (tetrahydrofuran (THF)) solvent extraction 20 hours, then used as the sample that is used to measure.Post is made of the A-801,802,803,804,805,806 and 807 that connects Showa Denko manufacturing, and molecular weight distribution is measured with the analytic curve of polystyrene standard resin.
The inventor has found that above-mentioned polymkeric substance has utmost point excellent characteristic as charge control agent.This will be shown in following examples.
At first, by embodiment A-1 new polymers and production method and the novel cpd that obtains by the present invention described to R-2.Use embodiment 1 to 40 and comparative example that the purposes of polymkeric substance of the present invention etc. is shown then.
New polymers of the present invention and compound and production method thereof are not limited only to embodiment shown below.
In following experiment, carry out the structure determination of gained compound.About NMR, 1H-NMR (FT-NMR:Bruker DPX400; Resonant frequency: 400MHz; Measure nucleic: 1H measures temperature: room temperature).
And, analyze it by fourier-transform infrared absorption (FT-IR) spectrum (NicoletAVATAR360FT-IR) and determine structure.
Unless stated otherwise, 1H-NMR measures and uses acetone-d 6Measure.
The molecular-weight average of resulting polymers is by gel permeation chromatography (GPC; Tosoh; Post, Polymer Laboratories PLgel 5 μ MIXED-C; Solvent, DMF/LiBr 0.1% (w/v), polystyrene conversion) estimate.Measure for acid number capacity (acid value volumetric), use potentiometric titration apparatus AT510 (making) by Kyoto Electronics Manufacturing.
＜embodiment A-0 〉
With reference to Macromolecules, 24,4310-4321 (1991) and Macromolecules, 26,2791-2795 (1993) co polystyrene and 4-vinyl benzoic acid.As a result, obtain content (M) than (mol%): (F)=93: 7 comprise by unitary multipolymer shown in the following formula (A-0):
The molecular-weight average of resulting polymers is number-average molecular weight Mn=22,000, and weight-average molecular weight Mw=52,000.
＜embodiment A-1 〉
With the polymkeric substance that obtains in the 1.5023g embodiment A-0, the three-necked flask that 0.8492g 2-aniline sulfonic acid is put into 200ml, add the 56.5ml pyridine, under nitrogen atmosphere, stir.Then, add the 2.57ml triphenylphosphine, and heated 6 hours down at 120 ℃.
After reaction finished, the evaporation pyridine added the 150ml chloroform to dissolve this polymkeric substance.Separation solution also with the salt acid elution of 600ml 2N, is collected the 1.2535g polymkeric substance after the solvent evaporation.With this polymer dissolution in THF and use distilled water and Virahol permeable membrane purifying.
Peak from the phenyl of 2-aniline sulfonic acid exists 1Move among the H-NMR result.As a result, the polymkeric substance of determining gained is for to comprise by unitary multipolymer shown in the following formula (A-1) than 6mol% with content:
Figure S2006800415696D00381
For resulting polymers, Mn=20,000, Mw=48,000.
Obtain this polymkeric substance of 50g by amplifying in proportion, and this compound is used for the preparation and the evaluation of toning agent as example compound A-1.
＜embodiment A-2 〉
The polymkeric substance that obtains in the 0.9777g embodiment A-1 is put into the 300mL flask, use 68.44ml chloroform and 17.11ml dissolve with methanol, and this mixture is cooled to 0 ℃.The hexane solution (product of Aldrich Company) that adds 3.00ml 2mol/L trimethyl silyl diazomethane was as esterifying agent, with this solution stirring 4 hours.Reaction by the evaporator evaporation solvent, is collected this polymkeric substance after finishing.In addition, add 68.44ml chloroform and 17.11ml methyl alcohol dissolving this polymkeric substance once more, and use the evaporator evaporation solvent.With the dissolving and the operation triplicate of evaporating solvent again.Obtain the 0.9552g polymkeric substance by vacuum-drying at the polymkeric substance of this collection.As 1H-NMR result observes the methyl proton peak 3 to 4ppm.Thus, the polymkeric substance of determining gained is for to comprise by unitary multipolymer shown in the following formula (A-2) than 6mol% with content:
Figure S2006800415696D00391
In addition, be clear that sulfonic group to be converted into the methylsulphonic acid ester group, because in acid number titration, do not observe point of equivalent derived from sulfonic acid.
For resulting polymers, Mn=19,000, Mw=45,000.
Obtain this polymkeric substance of 50g by amplifying in proportion, and prepare and evaluation as the toning agent that example compound A-2 is used for this compound.
＜Embodiment B-1 〉,＜Embodiment C-1 〉,＜embodiment D-1 〉,＜embodiment E-1 〉,＜embodiment F-1 〉,＜embodiment G-1 〉
With with embodiment A-1 in same way as with the polymkeric substance that obtains in the embodiment A-0 as raw material.
Except as table following as shown in the 1-1, by carry out with embodiment A-1 in the polymkeric substance of the synthetic Embodiment B-1 of identical operations, C-1, D-1, E-1, F-1 and G-1:
*Use thionamic acid
*Polymer loading
*The thionamic acid consumption
*The condensing agent consumption
*Solvent load.
Synthetic and analytical results is shown in table 1-2.
Table 1-1
Embodiment The thionamic acid that uses Polymer loading (g) Thionamic acid consumption (g) Condensing agent consumption (ml) Solvent load (ml)
(reference) A-1 The 2-aniline sulfonic acid 1.5023? 0.8492? 2.57? 56.50?
B-1? 4-anisidine-2-sulfonic acid 1.4996? 1.9894? 2.57? 56.50?
C-1? 2-amino phenyl sulfonyl acid phenenyl ester 3.0956? 5.0377? 5.30? 113.00?
D-1? The 3-aniline sulfonic acid 2.9954? 1.6933? 5.12? 113.00?
E-1? The 4-aniline sulfonic acid 1.5023? 1.6985? 5.14? 56.50?
F-1? 2-amino-1-naphthalene sulfonic aicd 1.5123? 1.1020? 5.17? 56.50?
G-1? Taurine 3.0024? 2.4529? 10.27? 113.00?
Table 1-2
Embodiment Introduce unitary structure *2? Introduce unitary ratio *1 (mol％)? Molecular weight Mw Molecular weight Mn Molecular weight Mw/Mn The amount (g) of the polymkeric substance of collecting
(reference) A-1 Chemical formula (A-1) 6? 48000? 20000? 2.4? 1.2535?
B-1? Chemical formula (B-1) 7? 47000? 21000? 2.2? 1.3023?
C-1? Chemical formula (C-1) 5? 49000? 20000? 2.5? 2.8842?
D-1? Chemical formula (D-1) 5? 48000? 20000? 2.4? 2.6789?
E-1? Chemical formula (E-1) 4? 47000? 20000? 2.4? 1.2333?
F-1? Chemical formula (F-1) 5? 48000? 21000? 2.3? 1.2256?
G-1? Chemical formula (G-1) 3? 50000? 19000? 2.6? 2.7002?
*1 from 1H-NMR result calculates
For B-1, C-1, D-1 and E-1, because derived from the peak migration of the phenyl of thionamic acid, determine the introducing of this structure and calculate this and introduce unitary ratio.
For F-1, because derived from the peak migration of the naphthyl of thionamic acid, determine the introducing of this structure and calculate this and introduce unitary ratio.
For G-1, because derived from the peak migration of the ethylidene of thionamic acid, determine the introducing of this structure and calculate this and introduce unitary ratio.
*2 introduce unitary structure is shown in structural formula 1.
Obtain this polymkeric substance of 50g by amplifying in proportion, and every kind of compound is used for the preparation and the evaluation of toning agent as example compound B-1, C-1, D-1, E-1, F-1 and G-1.
＜Embodiment B-2 〉,＜embodiment D-2 〉,＜embodiment E-2 〉,＜embodiment F-2 〉,＜embodiment G-2 〉
Except as table following as shown in the 1-3, by carry out with embodiment A-2 in the polymkeric substance of the synthetic Embodiment B-2 of identical operations, C-2, D-2, E-2, F-2 and G-2:
*Use other polymkeric substance to replace the polymkeric substance that obtains among the A-1 viewpoint as raw material
*Polymer loading
*The esterifying agent consumption
*Solvent load.
Synthetic and analytical results is shown in table 1-4.
Table 1-3
Embodiment Polymkeric substance as raw material Polymer loading (g) Esterifying agent consumption (ml) Chloroform consumption (ml) Methanol usage (ml)
(reference) A-2 Synthetic polymkeric substance in the embodiment A-1 0.9777? 3.00? 68.44? 17.11?
B-2? Synthetic polymkeric substance in the Embodiment B-1 1.0825? 2.91? 75.78? 18.94?
D-2? Synthetic polymkeric substance among the embodiment D-1 1.0023? 3.04? 70.16? 17.54?
E-2? Synthetic polymkeric substance in the embodiment E-1 0.9950? 3.09? 69.65? 17.41?
F-2? Synthetic polymkeric substance in the embodiment F-1 1.0236? 2.98? 71.65? 17.91?
G-2? Synthetic polymkeric substance among the embodiment G-1 1.0056? 3.17? 70.39? 17.60?
Table 1-4
Embodiment Introduce unitary structure *2? Introduce unitary ratio *1 (mol％)? Molecular weight Mw Molecular weight Mn Molecular weight Mw/Mn The amount (g) of the polymkeric substance of collecting
(reference) A-2 Chemical formula (A-2) 6? 45000? 19000? 2.4? 0.9552?
B-2? Chemical formula (B-2) 7? 46000? 19000? 2.4? 0.9332?
D-2? Chemical formula (D-2) 5? 47000? 19000? 2.5? 0.9265?
E-2? Chemical formula (E-2) 4? 45000? 19000? 2.4? 0.9666?
F-2? Chemical formula (F-2) 5? 46000? 20000? 2.3? 0.9335?
G-2? Chemical formula (G-2) 3? 48000? 18000? 2.7? 0.9546?
*1 from 1H-NMR result calculates
From calculating at 3 to 4ppm observed peaks derived from sulfamate.
*2 introduce unitary structure is shown in structural formula 1.
Obtain this polymkeric substance of 50g by amplifying in proportion, and every kind of compound is used for the preparation and the evaluation of toning agent as example compound B-2, D-2, E-2, F-2 and G-2.
Figure S2006800415696D00431
Figure S2006800415696D00441
＜embodiment H-1 〉
According to embodiment A-1 in identical document with vinylbenzene and the copolymerization of 4-vinyl benzoic acid.
As a result, than (mol%) (M) with content: (F)=obtain comprise by following formula (H-0) at 89: 11 unitary multipolymer is shown:
Use it for following experiment.
For resulting polymers, Mn=25,000, Mw=60,000.
Except as table following as shown in the 2-1, by carry out with embodiment A-1 in the identical operations synthetic polymer:
*Polymer loading
*The thionamic acid consumption
*The condensing agent consumption.
Synthetic and analytical results is shown in table 2-2.
Table 2-1
Embodiment Polymer loading (g) Thionamic acid consumption (g) Condensing agent consumption (ml)
(reference) A-1 1.5023? 0.8492? 2.57?
H-1? 1.5005? 1.4248? 4.31?
Table 2-2
Embodiment Introduce unitary structure *2? Introduce unitary ratio *1 (mol％)? Molecular weight Mw Molecular weight Mn Molecular weight Mw/Mn The amount (g) of the polymkeric substance of collecting
(reference) A-1 Chemical formula (A-1) 6? 48000? 20000? 2.4? 1.2535?
H-1? Chemical formula (H-1) 7? 58000? 23000? 2.5? 1.1856?
*1 from 1H-NMR result calculates
Because derived from the peak migration of the phenyl of thionamic acid, determine the introducing of this structure and calculate this and introduce unitary ratio.
*2 introduce unitary structure is shown in structural formula 2.
Obtain this polymkeric substance of 50g by amplifying in proportion, and prepare and evaluation as the toning agent that example compound H-1 is used for every kind of compound.
＜embodiment H-2 〉
Except as table following as shown in the 2-3, by carry out with embodiment A-2 in the identical operations synthetic polymer:
*Use the polymkeric substance that obtains among the H-1 to replace the polymkeric substance that obtains among the A-1
*Polymer loading
*The esterifying agent consumption
*Solvent load.
Synthetic and analytical results is shown in table 2-4.
Table 2-3
Embodiment Polymkeric substance as raw material Polymer loading (g) Esterifying agent consumption (ml) Chloroform consumption (ml) Methanol usage (ml)
(reference) A-2 Synthetic polymkeric substance in the embodiment A-1 0.9777? 3.00? 68.44? 17.11?
H-2? Synthetic polymkeric substance among the embodiment H-1 0.9990? 4.80? 69.93? 17.48?
Table 2-4
Embodiment Introduce unitary structure *2? Introduce unitary ratio *1 (mol％)? Molecular weight Mw Molecular weight Mn Molecular weight Mw/Mn The amount (g) of the polymkeric substance of collecting
(reference) A-2 Chemical formula (A-2) 6? 45000? 19000? 2.4? 0.9552?
H-2? Chemical formula (H-2) 6? 50000? 28000? 1.8? 0.9582?
*1 from 1H-NMR result calculates
From calculating at 3 to 4ppm observed peaks derived from sulphonate.
*2 introduce unitary structure is shown in structural formula 2.
Structural formula 2:
Figure S2006800415696D00461
Obtain this polymkeric substance of 50g and be referred to as example compound H-2 by amplifying in proportion.
＜example I-0 〉
With reference to Macromolecules, 32,1453-1462 (1999) is synthetic to be comprised by the unitary multipolymer shown in the following formula (I-0C) than (F)=15 (mol%) with content, and is used for following experiment:
Figure S2006800415696D00471
The molecular-weight average of resulting polymers is number-average molecular weight Mn=15,000, and weight-average molecular weight Mw=17,000.
＜example I-1 〉
Polymkeric substance that obtains in 1.4956g example I-0 and 0.8844g 2-aniline sulfonic acid are put into after the three-necked flask of 200ml, add the 113.0ml pyridine, under nitrogen atmosphere, stir this mixture, then, add the 2.68ml triphenylphosphine, and heated this mixture 6 hours down at 120 ℃.
After reaction finished, the evaporation pyridine added 150ml chloroform and 50ml methyl alcohol to dissolve this polymkeric substance.
Behind separation solution and the salt acid elution with 150ml 2N, the solvent of evaporation organic layer with 100ml washed with isopropyl alcohol solution, repeats twice, adds the 100ml hexane, washs and filter this mixture to collect the 1.2323g polymkeric substance.
With this polymer dissolution in THF and use distilled water and Virahol permeable membrane purifying.
Peak from the phenyl of 2-aniline sulfonic acid exists 1Move among the H-NMR result.As a result, the polymkeric substance of determining gained is for to comprise by unitary multipolymer shown in the following formula (I-1) than 12mol% with content:
For resulting polymers, Mn=13,000, Mw=15,000.
Obtain this polymkeric substance of 50g by repeating this preparation method, and this compound is used for the preparation and the evaluation of toning agent as example compound I-1.
＜example I-2 〉
Except as table following as shown in the 3-3, by carry out with embodiment A-2 in the identical operations synthetic polymer:
*Use the polymkeric substance that obtains among the I-1 to replace the polymkeric substance that obtains among the A-1
*Polymer loading
*The esterifying agent consumption
*Solvent load.
The results are shown in table 3-4.
Table 3-3
Embodiment Polymkeric substance as raw material Polymer loading (g) Esterifying agent consumption (ml) Chloroform consumption (ml) Methanol usage (ml)
(reference) A-2 Synthetic polymkeric substance in the embodiment A-1 0.9777? 3.00? 68.44? 17.11?
I-2? Synthetic polymkeric substance in the example I-1 0.9875? 59.96? 138.25? 34.56?
Table 3-4
Embodiment Introduce unitary structure *2? Introduce unitary ratio *1 (mol％)? Molecular weight Mw Molecular weight Mn Molecular weight Mw/Mn The amount (g) of the polymkeric substance of collecting
(reference) A-2 Chemical formula (A-2) 6? 45000? 19000? 2.4? 0.9552?
I-2? Chemical formula (I-2) 12? 14000? 12000? 1.2? 0.9324?
*1 from 1H-NMR result calculates
From calculating at 3 to 4ppm observed peaks derived from sulphonate.
*2 introduce unitary structure is shown in structural formula 3.
Structural formula 3:
Figure S2006800415696D00491
Obtain this polymkeric substance of 50g by repeating this preparation method, and use it for the preparation and the evaluation of toning agent as example compound I-2.
＜embodiment J-0 〉
With reference to Macromol.Chem.Phys, 195,3173-3187 (1994) and J.Am.Chem.Soc., 125, the segmented copolymer of 715-728 (2003) synthesizing styrene and 4-vinyl benzoic acid.As a result, obtain comprising by unitary segmented copolymer shown in the following formula (J-0) and be used for following test:
Figure S2006800415696D00492
M=210 in formula (J-0), n=21.
The molecular-weight average of resulting polymers is Mn=25,000, and Mw=30,000.
＜embodiment L-0 〉
With reference to Macromolecules, 24,4310-4321 (1991), Macromolecules, 26,2791-2795 (1993) obtains polymkeric substance as raw material by copolymerization of styrene and 4-vinyl benzoic acid.The polymkeric substance of the collecting permeable membrane purifying of molecular weight cut-off 2000.Then the polymkeric substance of collecting behind the dialysis purification is used the permeable membrane purifying of molecular weight cut-off (molecular cutoff) 3500.This polymkeric substance further uses the permeable membrane of molecular weight cut-off 8000 and 10000 with the same manner purifying.As a result, than (mol%) (M) with content: (F)=obtain comprise by following formula (L-0) shown in unitary multipolymer at 93: 7:
Figure S2006800415696D00501
Use it for following test.
For resulting polymers, Mn=23,000, Mw=32,000.
＜embodiment M-0 〉
With reference to Macromolecules, 24,4310-4321 (1991) and Macromolecules, 26,2791-2795 (1993) obtains polymkeric substance as raw material by copolymerization of styrene and 4-vinyl benzoic acid.The polymkeric substance of the collecting permeable membrane purifying of molecular weight cut-off 2000.Then the polymkeric substance of collecting behind the dialysis purification is used the permeable membrane purifying of molecular weight cut-off 3500.This polymkeric substance further uses the permeable membrane of molecular weight cut-off 8000 and 10000 with the same manner purifying.As a result, than (mol%) (M) with content: (F)=obtain comprise by following formula (M-0) shown in unitary multipolymer at 88: 12:
Figure S2006800415696D00502
Use it for following test.
For resulting polymers, Mn=26,000, Mw=36,000.
＜embodiment J-1 〉,＜embodiment K-1 〉,＜embodiment L-1 〉,＜embodiment M-1 〉
Except as table following as shown in the 4-1, by carry out with embodiment A-1 in the identical operations synthetic polymer:
*The polymer raw material that uses
*The thionamic acid that uses
*Polymer loading
*The thionamic acid consumption
*The condensing agent consumption
*Solvent load.
Synthetic and analytical results is shown in table 4-2.
Table 4-1
Embodiment Polymkeric substance as raw material The type of thionamic acid Polymer loading (g) Thionamic acid consumption (g) Condensing agent consumption (ml) Solvent load (ml)
(reference) A-1 Synthetic polymkeric substance in the embodiment A-0 The 2-aniline sulfonic acid 1.5023? 0.8492? 2.57? 56.50?
J-1? Synthetic polymkeric substance among the embodiment J-0 The 2-aniline sulfonic acid 1.5001? 2.1628? 6.55? 56.50?
K-1? Synthetic polymkeric substance among the embodiment J-0 The 4-aniline sulfonic acid 0.7502? 1.0816? 3.27? 28.25?
L-1? Synthetic polymkeric substance among the embodiment L-0 The 2-aniline sulfonic acid 1.4998? 0.8478? 2.57? 56.50?
M-1? Synthetic polymkeric substance among the embodiment M-0 The 2-aniline sulfonic acid 1.5022? 1.4265? 4.32? 56.50?
[0415]Table 4-2
Embodiment Introduce unitary structure *2? Introduce unitary ratio *1 (mol％)? Molecular weight Mw Molecular weight Mn Molecular weight Mw/Mn The amount (g) of the polymkeric substance of collecting
(reference) A-1 Chemical formula (A-1) 6? 48000? 20000? 2.4? 1.2535?
J-1? Chemical formula (J-1) 7? 29000? 23000? 1.3? 1.2003?
K-1? Chemical formula (K-1) 6? 29000? 22000? 1.3? 0.6852?
L-1? Chemical formula (L-1) 6? 30000? 22000? 1.4? 1.1563?
M-1? Chemical formula (M-1) 9? 32000? 23000? 1.4? 1.1023?
*1 from 1H-NMR result calculates
Owing to derive from the peak migration of the phenyl of thionamic acid, determine the introducing of this structure and calculate this and introduce unitary ratio.
*2 introduce unitary structure is shown in structural formula 4.
Obtain this polymkeric substance of 50g by repeating this preparation method, and use it for the preparation and the evaluation of toning agent as example compound J-1, K-1, L-1 and M-1.
＜embodiment J-2 〉,＜embodiment K-2 〉,＜embodiment L-2 〉,＜embodiment M-2 〉
Except as table following as shown in the 4-3, by carry out with embodiment A-2 in the identical operations synthetic polymer:
*Use the polymkeric substance that obtains among other polymkeric substance replacement A-1 as raw material
*Polymer loading
*The esterifying agent consumption
*Solvent load.
Synthetic and analytical results is shown in table 4-4.
Table 4-3
Embodiment Polymkeric substance as raw material Polymer loading (g) Esterifying agent consumption (ml) Chloroform consumption (ml) Methanol usage (ml)
(reference) A-2 Synthetic polymkeric substance in the embodiment A-1 0.9777? 3.00? 68.44? 17.11?
J-1? Synthetic polymkeric substance among the embodiment J-1 0.9950? 3.78? 69.65? 17.41?
K-1? Synthetic polymkeric substance among the embodiment K-1 1.0233? 3.83? 71.63? 17.91?
L-1? Synthetic polymkeric substance among the embodiment L-1 1.0231? 3.00? 71.62? 17.90?
M-1? Synthetic polymkeric substance among the embodiment M-1 1.0345? 4.86? 72.42? 18.10?
Table 4-4
Embodiment Introduce unitary structure *2? Introduce unitary ratio *1 (mol％)? Molecular weight Mw Molecular weight Mn Molecular weight Mw/Mn The amount (g) of the polymkeric substance of collecting
(reference) A-2 Chemical formula (A-2) 6? 45000? 19000? 2.4? 0.9552?
J-1? Chemical formula (J-2) 7? 28000? 23000? 1.2? 0.9021?
K-1? Chemical formula (K-2) 6? 28000? 21000? 1.3? 0.9124?
L-1? Chemical formula (L-2) 6? 29000? 21000? 1.4? 0.9389?
M-1? Chemical formula (M-2) 9? 31000? 22000? 1.4? 0.9586?
*1 from 1H-NMR result calculates
From calculating at 3 to the 4ppm observed peaks that derive from sulphonate.
*2 introduce unitary structure is shown in structural formula 4.
Structural formula 4:
Obtain this polymkeric substance of 50g by amplifying in proportion, and use it for the preparation and the evaluation of toning agent as example compound J-2, K-2, L-2 and M-2.
＜embodiment N-0 〉
With reference to Japanese Patent Application Laid-Open 2002-138111 and Macromolecules, 30, the synthetic monomer of 2016-2020 (1997) by chemical formula (N-0) expression:
Figure S2006800415696D00542
50.0g is dissolved in the 120ml ion exchanged water as the 4-aniline sulfonic acid of raw material.In addition, add therein 12.0g sodium hydroxide and with the mixture heating up to 40 of gained ℃ with dissolving.After the stirring, add the 100ml ion exchanged water, then water is evaporated.The dissolving again that will be in the 100ml ion exchanged water and the operation triplicate of evaporating solvent.
In this powder, add 25.0ml distilled water, 24.5g sodium bicarbonate and 15.0ml methyl alcohol, stirred 4 hours.
To wherein slowly dripping 33.3g the vinyl benzene formyl chloride is dissolved in solution among the 150mlTHF.
After being added dropwise to complete, this solution stirring is cooled to 0 ℃ in 30 minutes then, filters and collect crystal.And, it is used methanol wash, obtain the 10.5g monomer.
By 1The structure determination of gained compound is carried out in the H-NMR measurement.Polymerization below the monomer of this gained is used for.
＜embodiment N-1 〉
With the test tube that the monomer that obtains among the 0.4067g embodiment N-0 and 2.7ml vinylbenzene are put into 30mL, add 20ml DMSO with dissolving and carry out 12 hours nitrogen bubbles with deaeration.
After 41.2mg 2,2 '-azo in will being dissolved in 5.0ml DMSO two (isopropyl cyanide) adds in the test tube as initiator, stir down with this mixture heating up and at 70 ℃.After 9 hours, the polymkeric substance that obtains permeable membrane purifying, the monomeric homopolymer of unreacted monomer and chemical formula (N-0) is collected this polymkeric substance of 0.9681g thus by its water and salt acid elution are removed.Peak from monomeric phenyl structure exists 1Move among the H-NMR result.As a result, the polymkeric substance of definite gained is with content than (mol%) (NM) thus: (NF)=comprise by following formula (N-1) shown in unitary multipolymer at 95: 5:
For resulting polymers, Mn=21,000, Mw=36,000.Obtain this polymkeric substance of 50g by amplifying in proportion, and use it for the preparation and the evaluation of toning agent as example compound N-1.
＜embodiment N-2 〉
Except as table following as shown in the 5-1, by carry out with embodiment A-2 in the identical operations synthetic polymer:
*Use the polymkeric substance that obtains among the polymkeric substance replacement A-1 that obtains among the N-1 as raw material
*Polymer loading
*The esterifying agent consumption
*Solvent load.
Synthetic and analytical results is shown in table 5-2.
Table 5-1
Embodiment Polymkeric substance as raw material Polymer loading (g) Esterifying agent consumption (ml) Chloroform consumption (ml) Methanol usage (ml)
(reference) A-2 Synthetic polymkeric substance in the embodiment A-1 0.9777? 3.00? 68.44? 17.11?
N-2? Synthetic polymkeric substance among the embodiment N-1 0.9980? 2.19? 69.86? 17.47?
[0461]Table 5-2
Embodiment Introduce unitary structure *2? Introduce unitary ratio *1 (mol％)? Molecular weight Mw Molecular weight Mn Molecular weight Mw/Mn The amount (g) of the polymkeric substance of collecting
(reference) A-2 Chemical formula (A-2) 6? 45000? 19000? 2.4? 0.9552?
N-2? Chemical formula (N-2) 5? 35000? 20000? 1.8? 0.9325?
*1 from 1H-NMR result calculates
From calculating at 3 to the 4ppm observed peaks that derive from sulphonate.
*2 introduce unitary structure is shown in structural formula 5.
Structural formula 5:
Figure S2006800415696D00571
Obtain this polymkeric substance of 50g and be referred to as example compound N-2 by amplifying in proportion.
＜embodiment O-0 〉
The monomer that obtains among the embodiment N-0 makes the spent ion exchange resin desalination, with reference to SYNTHETIC COMMUNICATIONS, and 15 (12), 21,1057-1062 (1985) synthesizes following (O-0):
Figure S2006800415696D00581
3.5032g is put into flask by the desalinization compound shown in the chemical formula (N-0), 20ml trimethyl orthoformate with as the para benzoquinone (benzoquinone) of polymerization retarder, under nitrogen atmosphere 70 ℃ of heating 5 hours.With this reaction mixture cooling and under reduced pressure concentrated.With this mixture of 3L water washing, repeat twice, use the 3L hexane wash, repeat twice, be dissolved in again and also use anhydrous magnesium sulfate drying, evaporating solvent in the chloroform.
With 1H-NMR (FT-NMR:Bruker DPX400, resonant frequency: 400MHz measure nuclear: 1H, the solvent of use: CDCl 3, measure temperature: the structure of room temperature) carrying out the gained compound is determined.Because as 1H-NMR result observes the methyl proton peak 3 to 4ppm, clearly sulfonic group has been converted into the methylsulphonic acid ester group.
In addition, because Na exists with the amount that is lower than the ultimate analysis detection limit, show and carried out methyl-esterified.
And, also, clearly sulfonic group has been converted into the methylsulphonic acid ester group because of the point of equivalent of in by the acid number titration of using potentiometric titration apparatus AT510 (making), not observing from sulfonic acid by KyotoElectronics Manufacturing.This monomer is used for following polymerization.
＜embodiment O-2 〉
With the test tube that the monomer that obtains among the 0.3930g embodiment O-0 and 2.7ml vinylbenzene are put into 30mL, add 20ml DMSO with dissolving and carry out 12 hours nitrogen bubbles with deaeration.41.2mg 2, the 2 '-azo two (isopropyl cyanide) that is dissolved among the 5.0ml DMSO is added in the test tube, this mixture is heated down and stirs at 70 ℃.After 9 hours, with resulting polymers permeable membrane purifying, the monomeric homopolymer of unreacted monomer and chemical formula (O-0) is collected this polymkeric substance of 0.9658g by its water and salt acid elution are removed.Peak from monomeric phenyl structure exists 1Move among the H-NMR result.As a result, the polymkeric substance of definite gained is with content than (mol%) (OM) thus: (OF)=comprise by following formula (O-2) shown in unitary multipolymer at 95: 5:
Figure S2006800415696D00591
For the polymkeric substance of gained, Mn=20,000, Mw=35,000.Obtain this polymkeric substance of 50g by amplifying in proportion, and this compound is called example compound O-1.
＜embodiment P-2 〉
The polymkeric substance that obtains in the 0.9993g embodiment A-1 is dropped in the flask, add the 7.30g trimethyl orthoformate, stirred this mixture 8 hours down at 80 ℃.
After reaction finishes, this mixture is dropped in the 100ml hexane also by filtering collected polymer.In addition, be dissolved in it among 10ml THF and in the 100ml hexane, carry out redeposition, collect this polymkeric substance of 0.8700g.
As 1H-NMR result observes the methyl proton peak 3 to 4ppm.Thus, the polymkeric substance of determining gained is for to comprise by unitary multipolymer shown in the following formula (P-2) than 6mol% with content:
Figure S2006800415696D00601
Be apparent that sulfonic group to be converted into the methylsulphonic acid ester group, because do not observe point of equivalent from sulfonic acid by acid number titration.
For resulting polymers, Mn=17,000, Mw=43,000.
＜embodiment Q-2 〉
The polymkeric substance that obtains in the 1.0032g embodiment A-1 is dropped in the flask, add the 10.20g triethyl orthoformate, stirred this mixture 8 hours down at 100 ℃.
After reaction finishes, this mixture is added dropwise in the 100ml hexane also by filtering collected polymer.In addition, be dissolved in it among 10ml THF and in the 100ml hexane, carry out redeposition, collect this polymkeric substance of 0.8050g.
By 1The result of H-NMR, the polymkeric substance of determining gained is for to comprise by unitary multipolymer shown in the following formula (Q-2) than 6mol% with content:
Figure S2006800415696D00602
Be apparent that sulfonic group to be converted into the sulfonic acid ethoxycarbonyl, because do not observe point of equivalent from sulfonic acid by acid number titration.
For resulting polymers, Mn=18,000, Mw=46,000.
＜embodiment R-0 〉
With reference to Japanese Patent Application Laid-Open 2002-138111 and Macromolecules, 30, the synthetic monomer of 2016-2020 (1997) by chemical formula (R-0) expression:
Figure S2006800415696D00611
With 6.5g 2-aniline sulfonic acid and 8.9g triethylamine as material dissolution in 70mlTHF, this mixture of cooling and stirring in ice bath.To wherein little by little dripping, after being added dropwise to complete, this mixture was stirred 5 hours the vinyl benzene formyl chloride.After reaction finishes, add the 70ml ion exchanged water, with solvent evaporation.After separating this mixture and the salt acid elution with ethyl acetate and 70ml 4N, evaporating solvent carries out purifying with silicagel column, obtains the 8.0g monomer.
By 1The structure determination of gained compound is carried out in the H-NMR measurement. 1The H-NMR measuring result is shown in Fig. 1.
The gained monomer is used for following polymerization.
＜embodiment R-1 〉
The monomer and the 1.8ml vinylbenzene that obtain among the 303.3mg embodiment R-0 are put into three-necked flask, add 45.6ml THF and be used for dissolving, carry out nitrogen bubble with deaeration.
To add as 32.8mg 2, the 2 '-azo two (isopropyl cyanide) of initiator, mixture is heated down and stirs at 70 ℃.After 9 hours, the polymkeric substance water of gained and Virahol dialysis, further water and salt acid elution are collected the 1.5876g polymkeric substance thus. 1Among the H-NMR result, from the peak disappearance of the two keys of monomer, from the peak migration of monomeric phenyl structure.As a result, the polymkeric substance of definite gained is with content than (mol%) (RM) thus: (RF)=comprise by following formula (R-1) shown in unitary multipolymer at 93: 7:
Figure S2006800415696D00621
For resulting polymers, Mn=15,000, Mw=28,000.
＜embodiment R-2 〉
Except as table following as shown in the 6-1, by carry out with embodiment A-2 in the identical operations synthetic polymer:
*Use the polymkeric substance that obtains among the polymkeric substance replacement A-1 that obtains among the R-1 as raw material
*Polymer loading
*The esterifying agent consumption
*Solvent load.
Synthetic and analytical results is shown in table 6-2.
Table 6-1
Embodiment Polymkeric substance as raw material Polymer loading (g) Esterifying agent consumption (ml) Chloroform consumption (ml) Methanol usage (ml)
(reference) A-2 Synthetic polymkeric substance in the embodiment A-1 0.9777? 3.00? 68.44? 17.11?
R-2? Synthetic polymkeric substance among the embodiment R-1 0.9878? 2.96? 69.20? 17.30?
Table 6-2
Embodiment Introduce unitary structure *2? Introduce unitary ratio *1 (mol％)? Molecular weight Mw Molecular weight Mn Molecular weight Mw/Mn The amount (g) of the polymkeric substance of collecting
(reference) A-2 Chemical formula (A-2) 6? 45000? 19000? 2.4? 0.9552?
R-2? Chemical formula (R-2) 6? 27000? 16000? 1.8? 0.9120?
*1: from 1H-NMR result calculates
From calculating at 3 to the 4ppm observed peaks that derive from sulphonate.
*2: introduce unitary structure and be shown in structural formula 6.
Structural formula 6:
Figure S2006800415696D00631
＜embodiment S-0 〉
Use the monomer that obtains among the embodiment R-0 synthetic following (S-0):
Figure S2006800415696D00641
With 150ml chloroform and 50ml methyl alcohol add 6.0g by in the compound shown in the chemical formula (R-0) under nitrogen atmosphere, dissolving, and in ice bath, this mixture is cooled to 0 ℃.A little drips the hexane solution (product of Aldrich Company) of 2mol/L trimethyl silyl diazomethane, after being added dropwise to complete, this mixture is stirred 3 hours.After reaction finishes, add 300ml chloroform and 100ml methyl alcohol and be used for dissolving, evaporating solvent.Should operate triplicate, carry out purifying, obtain the 4.0g monomer with silicagel column.
1The H-NMR measuring result is shown in Fig. 2.
Because conduct 1H-NMR result observes the methyl proton peak 3 to 4ppm, clearly sulfonic group has been converted into the methylsulphonic acid ester group.
＜embodiment S-2 〉
The monomer and the 1.8ml vinylbenzene that obtain among the 317.4mg embodiment S-0 are put into three-necked flask, add 45.9ml THF and be used for dissolving, carry out nitrogen bubble with deaeration.
32.8mg 2,2 '-after azo two (isopropyl cyanides) adds as initiator, at 70 ℃ of following heated mixt and stir.After 9 hours, the polymkeric substance water of gained and Virahol dialysis, further water and salt acid elution are collected the 1.7600g polymkeric substance. 1Among the H-NMR result, from the peak disappearance of the two keys of monomer, from the peak migration of monomeric phenyl structure.As a result, the polymkeric substance of definite gained is with content than (mol%) (SM) thus: (SF)=comprise by following formula (R-2) shown in unitary multipolymer at 92: 8:
Figure S2006800415696D00651
For resulting polymers, Mn=21,000, Mw=34,000.
＜embodiment T-1 〉
Will be than (mol%) (M) with content: (F)=comprise by unit following formula (T-0) shown at 91: 9, number-average molecular weight Mn=63,000, weight-average molecular weight Mw=84,000 polymkeric substance are as raw material:
This polymkeric substance of 0.5g and 0.3597g 2-aniline sulfonic acid are put into three-necked flask, add the 4.0ml pyridine, under nitrogen atmosphere, stir this mixture, add the 1.10ml triphenylphosphine, and heated this mixture 6 hours down at 115 ℃.
After reaction finished, the evaporation pyridine added the 50ml chloroform to dissolve this polymkeric substance.Behind separation solution and the hydrochloric acid and 50ml water washing with 50ml 2N, evaporating solvent is collected this polymkeric substance.This polymkeric substance of 0.27g is separated, be dissolved in the 1.0ml chloroform and redeposition in the 200ml Virahol.The polymkeric substance dialyzer purifying of collecting.
1The H-NMR measuring result is shown in Fig. 3.
1Among the H-NMR result, disappear, from the peak migration of the phenyl structure of 2-aniline sulfonic acid from the peak of two keys.As a result, the polymkeric substance of determining gained thus is for to comprise by unitary multipolymer shown in the following formula (T-1) than (mol%) 6mol% with content:
Figure S2006800415696D00661
＜embodiment T-2 〉
The polymkeric substance that obtains among the 0.07969g embodiment T-1 is put into flask, add 2.0ml chloroform and 0.5ml methyl alcohol dissolving this polymkeric substance, and this mixture is cooled to 0 ℃.The hexane solution that adds 0.3ml 2mol/L trimethyl silyl diazomethane (product of AldrichCompany) stirs this mixture 4 hours as esterifying agent.Reaction by the evaporator evaporation solvent, is collected this polymkeric substance after finishing.In addition, add 8.0ml chloroform and 2.0ml methyl alcohol with dissolve polymer once more, and use the evaporator evaporation solvent.With the dissolving and the operation triplicate of evaporating solvent again.
Obtain the 0.08339g polymkeric substance by dry this polymkeric substance under vacuum in this collection.
1The H-NMR measuring result is shown in Fig. 4.
As 1H-NMR result observes the methyl proton peak 3 to 4ppm.Thus, the polymkeric substance of determining gained is for to comprise by unitary multipolymer shown in the following formula (T-2) than 6mol% with content:
Figure S2006800415696D00671
In addition, be apparent that sulfonic group to be converted into the methylsulphonic acid ester group, because in acid number titration, do not observe the point of equivalent that derives from sulfonic acid.
For resulting polymers, Mn=43,000, Mw=70,000.
(embodiment 1)
At first, with Na 3PO 4Aqueous solution adding is equipped with in the 2L four neck flasks of high speed agitator TK-homomixer, and it is adjusted into revolution 10, and 000rpm also is heated to 60 ℃.Lentamente with CaCl 2The aqueous solution joins wherein and comprises the dispersing agent C a that is insoluble in water with preparation 3(PO 4) 2Aqueous dispersions.Simultaneously, disperseed following composition 3 hours with ball mill, add 10 mass parts as 2,2 of polymerization starter '-azo two (2, the 4-methyl pentane nitrile) and 10 mass parts releasing agents (carnauba wax, 83 ℃ of fusing points), prepare polymerizable monomer composition.
*Styrene monomer: 82 mass parts
*EHA monomer: 18 mass parts
*Divinyl benzene monomer: 0.1 mass parts
*Cyan colorant (C.I. pigment Blue 15): 6 mass parts
*Polyethylene oxide resin (molecular weight 3,200, acid number 8): 5 mass parts
*Example compound H-2:2 mass parts
Below, with in the above aqueous dispersions for preparing of polymerizable monomer composition input of above gained and in maintenance revolution 10, granulation in the time of 000rpm.Then, when stirring this mixture with stirrer paddle (paddle mixing blade), it finished polymerization in 6 hours 80 ℃ of polymerizations then 65 ℃ of reactions 3 hours.Reaction is cooled off this suspension liquid after finishing, and is adding the sour dispersing agent C a that is slightly soluble in water with dissolving 3(PO 4) 2After, filter this mixture, wash with water also dry to obtain blue polymer particle (1).The particle size of the blue polymer particles of measuring with Coulter counter multi-sizer (product of CoulterCorporation) of gained (1) is weight average particle diameter 7.4 μ m, the amount of fine powder (particle in distributed number below the 3.17 μ m exist ratio) is 4.9%, in population.
Mix by doing in Henschel mixer, the blue polymer particle for preparing more than 100 mass parts adds the thin hydrophobic silica particle (BET:270m that 1.3 mass parts are used as hexamethyldisilazane (hexamethyldisilazane) processing of fluidity improver at home and abroad 2/ g).This is called the blue toner (1) of present embodiment.Then, with this blue toner of 7 mass parts (1) and the resin-coated magnetic ferrite carrier (median size: 45 μ m) mix the blue photographic developer (1) of two-pack that is used for magnetic brush development (magnetic brush developing) with preparation of 93 mass parts.
(embodiment 2 to 5)
Except replace example compound H-2 respectively with example compound B-1, F-1, M-1 and G-2, by with embodiment 1 in identical method obtain the blue toner (2) of embodiment 2 to 5 to (5).With with embodiment 1 in identical mode measure the characteristic of these toning agents, the results are shown in table 9.Use these toning agents, also with embodiment 1 in identical mode obtain the blue photographic developer of two-pack (2) of embodiment 2 to 5 to (5).
(comparative example 1)
Except the usage example compound not, with embodiment 1 in identical mode obtain the blue toner (6) of comparative example 1.With with embodiment 1 in identical mode measure the characteristic of this toning agent, the results are shown in table 7.Use this toning agent, also with embodiment 1 in identical mode obtain the blue photographic developer (6) of two-pack of comparative example 1.
＜estimate
The blue photographic developer (6) of two-pack that obtains in blue photographic developer (1) to (5) of the two-pack that obtains among the above embodiment 1 of following evaluation and the comparative example 1.
Use the method for aforesaid measurement carried charge, respectively ambient temperature and moisture (25 ℃, 60%RH) and hot and humid (30 ℃ 80%RH) measure to be stirred the carried charge of toning agent after 10 seconds and 300 seconds under the condition.The carried charge of the two-pack emptying that records is rounded to a decimal place and passes through following standard evaluation.The results are summarized in table 7.
[charging property]
AA: very good (20.0 μ C/g are following)
A: good (be higher than-20.0 μ C/g but below-10.0 μ C/g)
B: can be practical (be higher than-10.0 μ C/g but below-5.0 μ C/g)
C: can not practicality (being higher than-5.0 μ C/g).
(embodiment 6 to 10)
Except using 2.0 mass parts example compound B-2, L-1, H-1, J-2 and A-2 and replace the cyan colorant with yellow colorants (Hansa yellow G), the Yellow toner (1) by obtaining embodiment 6 to 10 as method identical among the embodiment 1 is to (5).With with embodiment 1 in identical mode measure the characteristic of these toning agents, the results are shown in table 7.Use these toning agents, also with embodiment 1 in identical mode obtain two-pack yellow developer (1) to (5).
(comparative example 2)
Replace the cyan colorant except usage example compound not and with yellow colorants (organic yellow (Hansayellow) G), with embodiment 1 in identical mode obtain the Yellow toner (6) of comparative example 2.With with embodiment 1 in identical mode measure the characteristic of these toning agents, the results are shown in table 7.Use this toning agent, also with embodiment 1 in identical mode obtain the two-pack yellow developer (6) of comparative example 2.
＜estimate
With with embodiment 1 in identical mode measurement be used for the two-pack yellow developer (6) that obtains in two-pack yellow developer (1) to (5) that embodiment 6 to 10 obtains and the comparative example 2 toning agent carried charge and estimate.The results are summarized in table 7.
(embodiment 11 to 15)
Except using 2.0 mass parts example compound K-2, C-1, G-1, I-2 and N-1 and replace the cyan colorant with carbon black (DBP oil absorbed dose 110mL/100g), by with embodiment 1 in identical method obtain the black toner (1) of embodiment 11 to 15 to (5).With with embodiment 1 in identical mode measure the characteristic of these toning agents, the results are shown in table 7.Use these toning agents, also with embodiment 1 in identical mode obtain bicomponent black photographic developer (1) to (5).
(comparative example 3)
Replace the cyan colorant except usage example compound not and with carbon black (DBP oil absorbed dose 110mL/100g), with embodiment 1 in identical mode obtain the black toner (6) of comparative example 3.With with embodiment 1 in identical mode measure the characteristic of this toning agent, the results are shown in table 7.Use this toning agent, also with embodiment 1 in identical mode obtain the bicomponent black photographic developer (6) of comparative example 3.
＜estimate
With with embodiment 1 in identical mode measurement be used for the bicomponent black photographic developer (6) that obtains in bicomponent black photographic developer (1) to (5) that embodiment 11 to 15 obtains and the comparative example 3 toning agent carried charge and estimate.The results are summarized in table 7.
(embodiment 16)
*Styrene-propene butyl acrylate copolymer resin (70 ℃ of second-order transition temperatures): 100 mass parts
*Magenta pigment (C.I. Pigment red 114): 5 mass parts
*Wax (low molecular weight polyethylene, 94 ℃ of fusing points): 7 mass parts
*Example compound N-2:2 mass parts
In biaxial extruder (L/D=30), mix and the above composition of melt kneading.With this blend in coarse crushing in hammer mill (hammer mill) after the cooling, and in airflow milling (jet mill) attritioning, carry out classification, thereby obtain magenta pigment particle (1) by this breaking method.The particle size of this magenta pigment particle (1) is weight average particle diameter 7.2 μ m, and the amount of fine powder is 5.7%, in population.
Mix by in Henschel mixer, doing, in 100 mass parts magenta pigment particles, add the thin hydrophobic silica particle (BET:250m that 1.5 mass parts are used as the hexamethyldisilazane processing of fluidity improver 2/ g), obtain magenta (red) colour toners (1) of present embodiment.Then, with this magenta of 7 mass parts (red) colour toners (1) and the resin-coated magnetic ferrite carrier (median size: 45 μ m) mix two-pack magenta (red) the look photographic developer (1) that is used for magnetic brush development (magnetic brush developing) with preparation of 93 mass parts.
(embodiment 17 to 20)
Except usage example compound F 17-hydroxy-corticosterone-2, I-1, K-1 and M-2, magenta (red) colour toners (2) by obtaining embodiment 17 to 20 as method identical among the embodiment 16 is to (5).With with embodiment 1 in identical mode measure the characteristic of these toning agents, the results are shown in table 7.Use these toning agents, also with embodiment 16 in identical mode obtain two-pack magenta (red) the look photographic developer (2) of embodiment 17 to 20 to (5).
(comparative example 4)
Except the usage example compound not, with embodiment 16 in identical mode obtain magenta (red) colour toners (6) of comparative example 4.With with embodiment 1 in identical mode measure the characteristic of this toning agent, the results are shown in table 7.Use this toning agent, also with embodiment 16 in identical mode obtain two-pack magenta (red) the look photographic developer (6) of comparative example 4.
＜estimate
With with embodiment 1 in identical mode measurement be used for two-pack magenta (red) the look photographic developer (6) that obtains in two-pack magenta (red) look photographic developer (1) to (5) that embodiment 17 to 20 obtains and the comparative example 4 toning agent carried charge and estimate.The results are summarized in table 7.
(embodiment 21 to 25)
Except using 2.0 mass parts example compound P-2, D-1, E-2, J-1 and L-2 and with carbon black (DBP oil absorbed dose 110mL/100g) the substitute red pigment, by with embodiment 16 in identical method obtain the black toner (7) of embodiment 21 to 25 to (11).With with embodiment 1 in identical mode measure the characteristic of these toning agents, the results are shown in table 7.Use these toning agents, also with embodiment 16 in identical mode obtain bicomponent black photographic developer (7) to (11).
(comparative example 5)
Except usage example compound not and with carbon black (DBP oil absorbed dose 110mL/100g) the substitute red pigment, with embodiment 16 in identical mode obtain the black toner (12) of comparative example 5.With with embodiment 1 in identical mode measure the characteristic of this toning agent, the results are shown in table 7.Use this toning agent, also with embodiment 16 in identical mode obtain the bicomponent black photographic developer (12) of comparative example 5.
＜estimate
With with embodiment 1 in identical mode measurement be used for the bicomponent black photographic developer (12) that obtains in bicomponent black photographic developer (7) to (11) that embodiment 21 to 25 obtains and the comparative example 5 toning agent carried charge and estimate.The results are summarized in table 7.
(embodiment 26)
*Vibrin: 100 mass parts
*Carbon black (DBP oil absorbed dose 110mL/100g): 5 mass parts
*Wax (low molecular weight polyethylene, 94 ℃ of fusing points): 7 mass parts
*Example compound E-1:2 mass parts
Following synthesizing polyester resin.Use 2 parts of dibutyltin oxides as catalyzer, 751 parts of bisphenol-A epoxy propane of polycondensation 2mol adducts, 104 part of four phthalandione and 167 parts of anhydrous trimellitic acids obtain having the vibrin of 125 ℃ of softening temperatures.
In biaxial extruder (L/D=30), mix and the above composition of melt kneading.This blend is in coarse crushing in hammer mill after the cooling, and in small, broken bits in airflow milling, carry out classification, thereby obtain this black colorant particle (13) by the method for pulverizing.The particle size of this black colorant particle (13) is weight average particle diameter 7.6 μ m, and the amount of fine powder is 4.8%, in population.
Mix by in Henschel mixer, doing, in 100 mass parts black colorant particles (13), add the thin hydrophobic silica particle (BET:250m with hexamethyldisilazane processing of 1.5 mass parts as fluidity improver 2/ g), obtain the black toner (13) of present embodiment.Then, with the black toner (13) of 7 mass parts gained and the resin-coated magnetic ferrite carrier (median size: 45 μ m) mix the bicomponent black photographic developer (13) that is used for magnetic brush development with preparation of 93 mass parts.
(embodiment 27 to 30)
Except replacing the example compound E-1 with example compound A-1, D-2, Q-2 and O-2 respectively, obtain the black toner (14) of embodiment 27 to 30 to (17) by the method identical with embodiment 26.With with embodiment 1 in identical mode measure the characteristic of these toning agents, the results are shown in table 7.Use these toning agents, also with embodiment 26 in identical mode obtain the bicomponent black photographic developer (14) of embodiment 27 to 30 to (17).
(comparative example 6)
Except the usage example compound not, with embodiment 26 in identical mode obtain the black toner (18) of comparative example 6.With with embodiment 1 in identical mode measure the characteristic of these toning agents, the results are shown in table 7.Use this toning agent, also with embodiment 26 in identical mode obtain the bicomponent black photographic developer (18) of comparative example 6.
＜estimate
With with embodiment 1 in identical mode measurement be used for the bicomponent black photographic developer (18) that obtains in bicomponent black photographic developer (13) to (17) that embodiment 26 to 30 obtains and the comparative example 6 toning agent carried charge and estimate.The results are summarized in table 7.
Table 7
(, magenta being called redness) for easy
(embodiment 31 to 36 and comparative example 7 to 12)
LBP5500 (being made by Canon Inc.) reequiped and be used for the evaluation of embodiment 31 to embodiment 36 and comparative example 7 to comparative example 12.
In these trials, by embodiment 1,6,11,16,21 and 26 and comparative example 1 to 6 in the cyan toner, Yellow toner, magenta toner or the black toner that obtain form toner image as photographic developer.
＜estimate
Above-mentioned condition and ambient temperature and moisture (25 ℃, 60%RH) and hot and humid (30 ℃, 80%RH) under, LBP5500 prints by repacking, print speed and be 8 pages (A4 sizes)/minute.
By using respectively and supplying with the toning agent of embodiment 1,6,11,16,21 and 26 and the toning agent of comparative example 1 to 6 one by one, under monochromatic intermittent mode, print output test.Estimate gained the printout image about and the following.Evaluation result is summarized in table 8.At this, intermittent mode paused 10 seconds for the every printing one page of developing apparatus wherein, to quicken the pattern of toner deterioration by the initial operation when restarting.
[printout picture appraisal]
1. image color
At common plain copying paper (75g/m 2) on print the predetermined number of pages of output, estimate based on compare with the initial pictures concentration degree of maintenance of final printout image.At this, use the reflective concentration meter of Macbeth (making) measurement image concentration by MacbethCorporation, measure the contrast starting point concentration and be 0.00 white portion the printout image relative concentration and be used for estimating.
AA: good (image color during final printout is more than 1.40)
A: good (image color during final printout is more than 1.35 but is lower than 1.40)
B: can accept (image color during final printout is more than 1.00 but is lower than 1.35)
C: unacceptable (image color during final printout is less than 1.00)
2. image hazes
At common plain copying paper (75g/m 2) on print the predetermined number of pages of output, estimate based on the complete white image when the final printout.Particularly, estimate by following method.Measure (by TOKYODENSHOKU CO., the REFLECTOMETER MODELTC-6DS that LTD makes) with the reflection density instrument.That is, will be expressed as Ds by the Schwellenwert of reflection density on full white region after the printing, the reflection density mean value of paper is expressed as Dr before the printing, (Ds-Dr) is determined by these values, thinks that this is the amount of hazing and passes through following standard evaluation.
AA: good (amount of hazing is more than 0% but is lower than 1.5%)
A: good (amount of hazing is more than 1.5% but is lower than 3.0%)
B: can practicality (amount of hazing is more than 3.0% but is lower than 5.0%)
C: impracticable (amount of hazing is more than 5.0%)
3. transfer printing
At common plain copying paper (75g/m 2) on print the predetermined number of pages that all black picture is used in output, estimate in the blank amount of final printout image epigraph by visual observation, and by following standard evaluation.
AA: good (almost not having blank the generation)
A: good (slightly)
B: can be practical
C: can not be practical
In addition, visual valuation embodiment 31 to embodiment 36 and comparative example 7 generation that photosensitive drums (photoconductive drum) or the lip-deep defective of intermediate transfer member, remaining toner are detained to the comparative example 12 and carry out after 5,000 pages printing the influence of output image (with the LBP5500 coupling) in image output.
In the system of the toning agent that uses embodiment 31 to embodiment 36, do not have the lip-deep defective of photosensitive drums or intermediate transfer member, do not observe generation that remaining toner is detained and with the LBP5500 good match.On the other hand, using comparative example 7 to any system of the toning agent of comparative example 12, to observe the delay of toning agent on photosensitive drums.And, using comparative example 7 to the system of the toning agent of comparative example 12, on intermediate transfer member, observe the delay and the surface imperfection of toning agent, image deflects also take place in longitudinal wire forms and cause the problem of mating with LBP5500 thus.
Table 8
(embodiment 37 to 39 and comparative example 13 to 15)
When carrying out embodiment 37 to 39 and comparative example 13 to 15, respectively with embodiment 1,6 and 11 and comparative example 1 to 3 in the toning agent that obtains as photographic developer.Repacking LBP5500 is as the device that forms image and use the replacement image forming apparatus thus by assembling recovering mechanism (the toning agent system of use collection).
As above, under ambient temperature and moisture (25 ℃, 60%RH) with continuous mode by supply with continuously toning agent print 8 pages of speed (A4 size)/minute under carry out 30,000 pages of printouts.
At this, continuous mode promotes the pattern that toning agent consumes for wherein not installing developing apparatus.
Measurement image concentration on the printout image of gained is with its weather resistance of following standard evaluation.In addition, observe the image on the 10th, 000 page and haze with following standard evaluation image.Meanwhile, after endurance test, observe the state of each device that constitutes LBP5500, also estimate the coupling between each device and each above toning agent.These the results are summarized in table 9.
[change of image color during endurance test]
At common plain copying paper (75g/m 2) on print the predetermined number of pages of output, estimate based on the concentration degree that keeps of on final printout image, comparing with initial pictures.At this, use the reflective concentration meter of Macbeth (making) measurement image concentration by Macbeth Corporation, measure the contrast starting point concentration and be 0.00 white portion the printout image relative concentration and be used for estimating.
AA: good (image color during final printout is not less than 1.40)
A: good (image color during final printout is more than 1.35 but is lower than 1.40)
B: can accept (image color during final printout is more than 1.00 but is lower than 1.35)
C: unacceptable (image color during final printout is for being lower than 1.00)
[image hazes]
At common plain copying paper (75g/m 2) on print the predetermined number of pages of output, when final printout, estimate based on complete white image.Estimate by the method for using reflective concentration meter (by TOKYO DENSHOKU CO., the REFLECTOMETER MODEL TC-6DS that LTD makes).
[the image forming apparatus coupling is estimated]
1. mate with development sleeve
After the printout off-test, the visual valuation remaining toner is at the delay state on development sleeve surface with to printing the influence of output image.
AA: good (not taking place)
A: good (almost not taking place)
B: can practicality (exist and be detained, but image is not almost had influence)
C: impracticable (a large amount of delay and the generation of inhomogeneous image)
2. mate with photosensitive drums
The generation that defective on the visual valuation photosensitive drums, remaining toner are detained and to printing the influence of output image.
AA: good (not taking place)
A: good (observe minor defects but image is not had influence)
B: can practicality (take place to be detained and defective, but image is not almost had influence)
C: impracticable (being detained and appearing at the defective of the image of longitudinal wire form in a large number)
3. with the coupling of fixation facility
Observe the surperficial and average of photographic fixing film, and estimate weather resistance with the delay result of superficiality and remaining toner.
Superficiality
In the printout test back visual observation lip-deep defective of photographic fixing film or scratch and evaluation.
AA: good (not taking place)
A: good (almost not taking place)
B: can be practical
C: impracticable
(2) the delay state of remaining toner
After the printout off-test, the delay state of visual observation and evaluation remaining toner on photographic fixing film surface.
AA: good (not taking place)
A: good (almost not taking place)
B: can be practical
C: impracticable
Figure S2006800415696D00801
(embodiment 40)
Dismounting is used for the toning agent recovering mechanism of the LBP5500 of embodiment 37 to 39 and comparative example 13 to 15, with printout speed change into 16 pages (A4 sizes)/minute.Identical among other condition and the embodiment 37, the blue toner (1) by continuous supply embodiment 1 prints output test with continuous mode.
At this, continuous mode promotes the pattern that toning agent consumes for wherein not installing developing apparatus.
For identical project in embodiment 37 to 39 and the comparative example 13 to 15, estimate gained the printout image and with the coupling of employed LBP5500.As a result, in every, all obtain good result.
Polymkeric substance of the present invention can be applicable to, and for example, is included in the charge control agent of the toning agent that is used for Electronic Photographing Technology.
The application requires it all to be introduced with for referencial use at this in the right of priority of the Japanese patent application 2005-328179 of submission on November 11st, 2005.

Claims (4)

1. polymkeric substance, it has the unit by chemical formula (1) expression:
Wherein R represents-A 1-SO 2R 1R 1wAnd R 1XBe hydrogen atom independently of one another; R 1yBe CH 3Base or hydrogen atom;
A 01Aromatic ring structure for replacement or non-replacement;
A 1For replacing or the aliphatic hydrocrbon structure of non-replacement or the aromatic ring structure of replacement or non-replacement;
R 1Be OH, ONa, OK or OR 1aR 1aFor replacing or the aliphatic hydrocrbon structure of non-replacement or the aromatic ring structure of replacement or non-replacement.
2. polymkeric substance, it is unit according to claim 1 and the monomeric unitary multipolymer of derived from ethylene base class by chemical formula (101) expression:
Figure FSB00000317980600012
R wherein 101wAnd R 101xBe hydrogen atom independently of one another;
R 101yBe CH 3Base or hydrogen atom; R 101For following one of any: the aromatic ring structure of aliphatic hydrocrbon structure, replacement or the non-replacement of hydrogen atom, replacement or non-replacement ,-CO-R 101a,-O-R 101b,-COO-R 101c,-OCO-R 101d,-CONR 101eR 101f, or-CN; R 101a, R 101b, R 101c, R 101d, R 101eAnd R 101fBe the aliphatic hydrocrbon structure of hydrogen atom, replacement or non-replacement or the aromatic ring structure of replacement or non-replacement independently of one another.
3. compound by chemical formula (201) expression:
Figure FSB00000317980600021
Wherein R represents-A 201-SO 2R 201R 201wAnd R 201XBe hydrogen atom independently of one another; R 201yBe CH 3Base or hydrogen atom;
A 0201Aromatic ring structure for replacement or non-replacement;
A 201For replacing or the aliphatic hydrocrbon structure of non-replacement or the aromatic ring structure of replacement or non-replacement;
R 201Be OH, ONa, OK or OR 201aR 201aFor replacing or the aliphatic hydrocrbon structure of non-replacement or the aromatic ring structure of replacement or non-replacement.
4. toning agent that is used for developing electrostatic latent image, it comprises resin glue, tinting material and polymkeric substance according to claim 1.
CN2006800415696A 2005-11-11 2006-11-10 Polymer having sulfonic acid group or sulfonic acid ester group and amide group, and toner for developing electrostatic latent image having the polymer Expired - Fee Related CN101305023B (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP328179/2005 2005-11-11
JP2005328179 2005-11-11
PCT/JP2006/322906 WO2007055414A1 (en) 2005-11-11 2006-11-10 Polymer having sulfonic acid group or sulfonic acid ester group and amide group, and toner for developing electrostatic latent image having the polymer

Publications (2)

Publication Number Publication Date
CN101305023A CN101305023A (en) 2008-11-12
CN101305023B true CN101305023B (en) 2011-03-02

Family

ID=37606916

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2006800415696A Expired - Fee Related CN101305023B (en) 2005-11-11 2006-11-10 Polymer having sulfonic acid group or sulfonic acid ester group and amide group, and toner for developing electrostatic latent image having the polymer

Country Status (6)

Country Link
US (1) US7935771B2 (en)
EP (1) EP1951769B1 (en)
KR (1) KR100989499B1 (en)
CN (1) CN101305023B (en)
DE (1) DE602006005841D1 (en)
WO (1) WO2007055414A1 (en)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070117945A1 (en) * 2005-11-11 2007-05-24 Canon Kabushiki Kaisha Novel polymer, charge control agent, and toner for developing electrostatic latent images
JP4565054B2 (en) * 2009-02-27 2010-10-20 キヤノン株式会社 Black toner
JP4565053B2 (en) 2009-02-27 2010-10-20 キヤノン株式会社 Magenta toner
WO2010098226A1 (en) * 2009-02-27 2010-09-02 Canon Kabushiki Kaisha Yellow toner
JP5658550B2 (en) * 2009-12-28 2015-01-28 キヤノン株式会社 toner
KR20130136550A (en) * 2011-03-30 2013-12-12 캐논 가부시끼가이샤 Polymerizable monomer, polymeric compound, charge control agent containing the polymeric compound, and developer bearing member and toner which contain the charge control agent
US8574801B2 (en) 2011-05-18 2013-11-05 Canon Kabushiki Kaisha Toner
JP6053336B2 (en) 2011-06-03 2016-12-27 キヤノン株式会社 Toner and toner production method
WO2012165638A1 (en) 2011-06-03 2012-12-06 キヤノン株式会社 Toner
JP5836888B2 (en) 2011-06-03 2015-12-24 キヤノン株式会社 toner
TWI461864B (en) 2011-06-03 2014-11-21 Canon Kk Toner
US9823595B2 (en) 2015-06-30 2017-11-21 Canon Kabushiki Kaisha Toner
US9798256B2 (en) 2015-06-30 2017-10-24 Canon Kabushiki Kaisha Method of producing toner
JP2017083822A (en) 2015-10-29 2017-05-18 キヤノン株式会社 Method for manufacturing toner and method for manufacturing resin particle
US10409180B2 (en) 2017-02-13 2019-09-10 Canon Kabushiki Kaisha Resin fine particles, method of producing resin fine particles, method of producing resin particles, and method of producing toner
US10747136B2 (en) 2018-04-27 2020-08-18 Canon Kabushiki Kaisha Toner
US11256187B2 (en) 2019-07-25 2022-02-22 Canon Kabushiki Kaisha Process cartridge and electrophotographic apparatus
JP7336293B2 (en) 2019-07-25 2023-08-31 キヤノン株式会社 toner
JP7350553B2 (en) 2019-07-25 2023-09-26 キヤノン株式会社 toner
JP7328048B2 (en) 2019-07-25 2023-08-16 キヤノン株式会社 toner
JP7350554B2 (en) 2019-07-25 2023-09-26 キヤノン株式会社 toner
JP7321810B2 (en) 2019-07-25 2023-08-07 キヤノン株式会社 toner
JP7458915B2 (en) 2020-06-25 2024-04-01 キヤノン株式会社 toner
US11822286B2 (en) 2021-10-08 2023-11-21 Canon Kabushiki Kaisha Process cartridge and electrophotographic apparatus

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1201167A (en) * 1997-06-03 1998-12-09 莱克斯马克国际公司 Dry xerographic toners and developers
US5962178A (en) * 1998-01-09 1999-10-05 Xerox Corporation Sediment free toner processes
EP1241531A2 (en) * 2001-03-15 2002-09-18 Canon Kabushiki Kaisha Toner, image forming method and process cartridge
CN1381771A (en) * 2001-04-03 2002-11-27 株式会社理光 Tone agent, developer, image forming method and image forming device
WO2004061529A1 (en) * 2002-12-27 2004-07-22 Canon Kabushiki Kaisha Novel polyhydroxyalkanoate having amide, sulfonic acid or sulfonate ester group, charge control agent and toner

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1036700A (en) * 1965-03-26 1966-07-20 Tanabe Seiyaku Co Organic pigment
DE1595698C3 (en) * 1966-12-05 1974-08-01 Bayer Ag, 5090 Leverkusen Process for the preparation of acrylonitrile copolymers containing sulfonic acid amide groups
US3717687A (en) * 1971-03-24 1973-02-20 Lubrizol Corp Composition and method of imparting premanent press and soil release properties to fabrics
JPS4963419A (en) * 1972-10-18 1974-06-19
US4490308A (en) * 1983-06-30 1984-12-25 Nalco Chemical Company New water-soluble sulfonated monomers
US4812544A (en) * 1985-09-10 1989-03-14 The Lubrizol Corporation Method of producing polymers of amido-sulfonic acid monomers with high energy agitators
US5212270A (en) * 1990-03-15 1993-05-18 The Lubrizol Corporation Compositions suitable for imparting wetting characteristics to fabrics, and fabrics treated with same
DE4322884A1 (en) * 1992-10-09 1994-04-14 Bayer Ag Biologically active polymers
US5994430A (en) * 1997-04-30 1999-11-30 Clariant Finance Bvi) Limited Antireflective coating compositions for photoresist compositions and use thereof
JP2002138111A (en) 2000-11-02 2002-05-14 Daicel Chem Ind Ltd Complexed sugar modified polystyrene
JP2002351147A (en) 2001-05-30 2002-12-04 Fujikura Kasei Co Ltd Charge control agent and electrophotographic negative charge toner
US7252917B2 (en) 2003-03-10 2007-08-07 Canon Kabushiki Kaisha Dry toner, method for producing dry toner, and method for forming an image
US7094848B2 (en) * 2003-05-13 2006-08-22 Exxonmobil Chemical Patents Inc. Olefin polymerization catalyst system
CN1965002B (en) 2004-05-12 2010-05-05 佳能株式会社 Polymer having sulfonic acid group or sulfonic ester group and amide group, and method of producing the same
US7638194B2 (en) 2004-06-25 2009-12-29 Canon Kabushiki Kaisha Developer carrying member, and developing assembly
US7399568B2 (en) 2004-06-25 2008-07-15 Canon Kabushiki Kaisha Carrier for electrophotographic developer
US8110329B2 (en) 2005-11-11 2012-02-07 Canon Kabushiki Kaisha Charge controlling agent and toner
KR101045739B1 (en) 2005-11-11 2011-06-30 캐논 가부시끼가이샤 Resin for toner and toner

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1201167A (en) * 1997-06-03 1998-12-09 莱克斯马克国际公司 Dry xerographic toners and developers
US5962178A (en) * 1998-01-09 1999-10-05 Xerox Corporation Sediment free toner processes
EP1241531A2 (en) * 2001-03-15 2002-09-18 Canon Kabushiki Kaisha Toner, image forming method and process cartridge
CN1381771A (en) * 2001-04-03 2002-11-27 株式会社理光 Tone agent, developer, image forming method and image forming device
WO2004061529A1 (en) * 2002-12-27 2004-07-22 Canon Kabushiki Kaisha Novel polyhydroxyalkanoate having amide, sulfonic acid or sulfonate ester group, charge control agent and toner

Also Published As

Publication number Publication date
US20090162773A1 (en) 2009-06-25
EP1951769B1 (en) 2009-03-18
EP1951769A1 (en) 2008-08-06
US7935771B2 (en) 2011-05-03
CN101305023A (en) 2008-11-12
KR20080067006A (en) 2008-07-17
KR100989499B1 (en) 2010-10-22
DE602006005841D1 (en) 2009-04-30
WO2007055414A1 (en) 2007-05-18

Similar Documents

Publication Publication Date Title
CN101305023B (en) Polymer having sulfonic acid group or sulfonic acid ester group and amide group, and toner for developing electrostatic latent image having the polymer
CN1965002B (en) Polymer having sulfonic acid group or sulfonic ester group and amide group, and method of producing the same
EP3309619B1 (en) Toner and method for producing toner
US8093342B2 (en) Polymer, charge control agent, and toner for developing electrostatic latent images
JP5159087B2 (en) Charge control agent and electrostatic image developing toner
CA2746193C (en) Continuous process for producing toner using an oscillatory flow continuous reactor
JP2023018650A (en) Latexes and related compositions
JP2023018651A (en) toner
JP4996060B2 (en) Charge control agent containing polymer having sulfonate group and amide group, toner for developing electrostatic image using the same, image forming method and image forming apparatus
JP2007154177A (en) Polymer, charge controller and static charge developing toner
JP2007156457A (en) Charge controlling agent and electrostatic image developing toner
US11760845B2 (en) Method for producing resin particle dispersion, method for producing toner for electrostatic image development, and toner for electrostatic image development
EP3492986B1 (en) Magenta toner
JP5328097B2 (en) Polymer having sulfonic acid group or sulfonic acid ester group and amide group, and electrostatic image developing toner having the polymer
JP6478701B2 (en) Toner and toner production method
KR100841190B1 (en) Polymer having a sulfonic group or a sulfonate group and an amide group and method of producing same
JP2008260890A (en) Polymer having amido group, sulfonic acid group, or its derivative, charge controlling agent and toner
JP5737308B2 (en) Toner for electrostatic image development
JP2006055781A (en) Emulsifier, emulsion composition, capsulated toner composition, image forming method, process cartridge and electrograph device
JPH09258478A (en) Production of resin for toner and electrostatic charge image developing toner using the same
JPH09258477A (en) Production of resin for toner and electrostatic charge image developing toner using the same

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20110302

Termination date: 20201110

CF01 Termination of patent right due to non-payment of annual fee